Large

We're on a journey to forever caring.

It’s our promise to giving patients and healthcare providers the support they need as we bring  to life our vision of pioneering trusted medical solutions to improve the lives we touch. We’re focussed on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care   and infusion care.

Around the world, it's our people who are driving our business with    real momentum. Join us, and whatever your role, you’ll be pushed and challenged every day. You’ll be supported too, empowered to share new ideas    and drive change where it matters most. 

The sense of pride is powerful. It’s shared. And knowing what you do really matters will inspire you to deliver your very best. 

Science & Healthcare

Convatec

Pioneering trusted medical solutions to improve the lives we touch

You need a relevant degree, CAD proficiency (SolidWorks), experience in multiple projects, comfort with intimate body design, and effective English communication skills.

You will design and develop medical devices, collaborate on technical challenges, create 3D models, prototype, conduct testing, analyze data, and maintain documentation while ensuring compliance and engaging stakeholders.

Research & Development

Engineering

Chester

Liverpool

Wrexham

Salford

Birmingham

Manchester

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com Our search for better is changing the lives of our customers. It’s changing the careers of our people too – creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring as an R&D Engineer, and you won’t either. The role of R&D Engineer within ConvaTec’ Continence Care New Product Development Team is both a varied and demanding role. This Engineer will be part of an experienced international team developing products from idea conception, design development and product testing through to process development, design validation and product launch. Key Responsibilities: * Contribute to the Design and Development of medical devices from Concept to launch. * Through collaboration with multifunctional teams, support discussions to resolve technical / scientific challenges to support new product development of Continence Care medical devices. * Identifying & generating new Intellectual Property (IP), translating novel ideas into valuable & protectable IP and evaluating the IP landscape. * Direct creation of new concepts via 3D models & assemblies in CAD/CAM software (Solidworks). * Close collaboration with the cross functional process development team utilising Design for Manufacturing and Design for Assembly methodologies to develop robust designs suitable for manufacturing processes including plastic injection moulding, thermoforming etc * Develop ideas and designs with a focus on usability and user centric design. * Resolve concept ideas to practice through prototyping and / or other rapid simulation techniques. * Scope plan and execute / coordinate testing of prototypes. * Using existing templates, record and report experimental data. This includes reporting of the test procedure, presentation / analysis (including statistical analysis, e.g. Design of Experiments, etc.) of data and formulating conclusions and recommendations as a basis for further discussion and research. * Communicate technical data including conclusions and recommendations to the wider team, make proposals and recommendations to progress the projects forward based on the analysis of this data. * Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. * Maintain overall expertise by keeping updated on engineering advancements through publications, patents, university / industrial contacts and vendor discussions. * Work effectively and proactively engage with key stakeholders to manage expectations and deliver on commitments; Understand needs and requirements across multiple functions, manage relationships to ensure effective execution. * Work collaboratively across the organisation and support colleagues to achieve shared goals and objectives. * Role models behaviours appropriate to our values. * Maintain compliance with HSE regulations. * Maintain compliance with QMS. About You: * Qualified to degree level in a relevant engineering related subject preferably Mechanical or Design Engineering. * Experience in a variety of projects; ability to work on a number of teams and projects in tandem. * Comfortable with human body discussions and designing solutions of intimate parts of human body. * Ability to use CAD software packages (SolidWorks) is essential. * Demonstrable experience with knowledge of mechanical / design engineering is essential. * Experience in designing and developing plastic moulded components is desirable. * Experience in a R&D medical devices environment and design control is desirable. * Experience of Process Validation activities (FAT, SAT, IQ, OQ, PQ activities) is desirable. * Ability to communicate effectively in English (verbal and written) is essential. Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before. This is a big step forward. This is work that’ll move you. #WeAreConvatec Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. Equal opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a Convatec employee? If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more aboutConvatec, please visit http://www.convatecgroup.comOur search for better is changing the lives of our customers. It’s changing the careers of our people too – creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring as an R&D Engineer, and you won’t either.The role of R&D Engineer within ConvaTec’ Continence Care New Product Development Team is both a varied and demanding role. This Engineer will be part of an experienced international team developing products from idea conception, design development and product testing through to process development, design validation and product launch.Key Responsibilities: * Contribute to the Design and Development of medical devices from Concept to launch. * Through collaboration with multifunctional teams, support discussions to resolve technical / scientific challenges to support new product development of Continence Care medical devices. * Identifying & generating new Intellectual Property (IP), translating novel ideas into valuable & protectable IP and evaluating the IP landscape. * Direct creation of new concepts via 3D models & assemblies in CAD/CAM software (Solidworks). * Close collaboration with the cross functional process development team utilising Design for Manufacturing and Design for Assembly methodologies to develop robust designs suitable for manufacturing processes including plastic injection moulding, thermoforming etc * Develop ideas and designs with a focus on usability and user centric design. * Resolve concept ideas to practice through prototyping and / or other rapid simulation techniques. * Scope plan and execute / coordinate testing of prototypes. * Using existing templates, record and report experimental data. This includes reporting of the test procedure, presentation / analysis (including statistical analysis, e.g. Design of Experiments, etc.) of data and formulating conclusions and recommendations as a basis for further discussion and research. * Communicate technical data including conclusions and recommendations to the wider team, make proposals and recommendations to progress the projects forward based on the analysis of this data. * Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. * Maintain overall expertise by keeping updated on engineering advancements through publications, patents, university / industrial contacts and vendor discussions. * Work effectively and proactively engage with key stakeholders to manage expectations and deliver on commitments; Understand needs and requirements across multiple functions, manage relationships to ensure effective execution. * Work collaboratively across the organisation and support colleagues to achieve shared goals and objectives. * Role models behaviours appropriate to our values. * Maintain compliance with HSE regulations. * Maintain compliance with QMS.         About You: * Qualified to degree level in a relevant engineering related subject preferably Mechanical or Design Engineering. * Experience in a variety of projects; ability to work on a number of teams and projects in tandem. * Comfortable with human body discussions and designing solutions of intimate parts of human body. * Ability to use CAD software packages (SolidWorks) is essential. * Demonstrable experience with knowledge of mechanical / design engineering is essential. * Experience in designing and developing plastic moulded components is desirable. * Experience in a R&D medical devices environment and design control is desirable. * Experience of Process Validation activities (FAT, SAT, IQ, OQ, PQ activities) is desirable. * Ability to communicate effectively in English (verbal and written) is essential.         Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before.This is a big step forward.This is work that’ll move you.#WeAreConvatecBeware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

R&D Engineer - Convatec

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Group revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about&lt;br&gt;&lt;br&gt;Convatec, please visit http://www.convatecgroup.com&lt;br&gt;&lt;br&gt;Our search for better is changing the lives of our customers. It’s changing the careers of our people too – creating new challenges and opportunities all the time. We’re a business that never stands still. Join us on our journey to #ForeverCaring as an R&amp;amp;D Engineer, and you won’t either.&lt;br&gt;&lt;br&gt;The role of R&amp;amp;D Engineer within ConvaTec’ Continence Care New Product Development Team is both a varied and demanding role. This Engineer will be part of an experienced international team developing products from idea conception, design development and product testing through to process development, design validation and product launch.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Key Responsibilities: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Contribute to the Design and Development of medical devices from Concept to launch. &lt;/li&gt;&lt;li&gt;Through collaboration with multifunctional teams, support discussions to resolve technical / scientific challenges to support new product development of Continence Care medical devices. &lt;/li&gt;&lt;li&gt;Identifying &amp;amp; generating new Intellectual Property (IP), translating novel ideas into valuable &amp;amp; protectable IP and evaluating the IP landscape.&lt;/li&gt;&lt;li&gt;Direct creation of new concepts via 3D models &amp;amp; assemblies in CAD/CAM software (Solidworks).&lt;/li&gt;&lt;li&gt;Close collaboration with the cross functional process development team utilising Design for Manufacturing and Design for Assembly methodologies to develop robust designs suitable for manufacturing processes including plastic injection moulding, thermoforming etc&lt;/li&gt;&lt;li&gt;Develop ideas and designs with a focus on usability and user centric design. &lt;/li&gt;&lt;li&gt;Resolve concept ideas to practice through prototyping and / or other rapid simulation techniques.&lt;/li&gt;&lt;li&gt;Scope plan and execute / coordinate testing of prototypes. &lt;/li&gt;&lt;li&gt;Using existing templates, record and report experimental data. This includes reporting of the test procedure, presentation / analysis (including statistical analysis, e.g. Design of Experiments, etc.) of data and formulating conclusions and recommendations as a basis for further discussion and research. &lt;/li&gt;&lt;li&gt;Communicate technical data including conclusions and recommendations to the wider team, make proposals and recommendations to progress the projects forward based on the analysis of this data. &lt;/li&gt;&lt;li&gt;Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. &lt;/li&gt;&lt;li&gt;Maintain overall expertise by keeping updated on engineering advancements through publications, patents, university / industrial contacts and vendor discussions. &lt;/li&gt;&lt;li&gt;Work effectively and proactively engage with key stakeholders to manage expectations and deliver on commitments; Understand needs and requirements across multiple functions, manage relationships to ensure effective execution. &lt;/li&gt;&lt;li&gt;Work collaboratively across the organisation and support colleagues to achieve shared goals and objectives. &lt;/li&gt;&lt;li&gt;Role models behaviours appropriate to our values. &lt;/li&gt;&lt;li&gt;Maintain compliance with HSE regulations. &lt;/li&gt;&lt;li&gt;Maintain compliance with QMS. &lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;About You: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Qualified to degree level in a relevant engineering related subject preferably Mechanical or Design Engineering. &lt;/li&gt;&lt;li&gt;Experience in a variety of projects; ability to work on a number of teams and projects in tandem. &lt;/li&gt;&lt;li&gt;Comfortable with human body discussions and designing solutions of intimate parts of human body.&lt;/li&gt;&lt;li&gt;Ability to use CAD software packages (SolidWorks) is essential. &lt;/li&gt;&lt;li&gt;Demonstrable experience with knowledge of mechanical / design engineering is essential. &lt;/li&gt;&lt;li&gt;Experience in designing and developing plastic moulded components is desirable. &lt;/li&gt;&lt;li&gt;Experience in a R&amp;amp;D medical devices environment and design control is desirable. &lt;/li&gt;&lt;li&gt;Experience of Process Validation activities (FAT, SAT, IQ, OQ, PQ activities) is desirable. &lt;/li&gt;&lt;li&gt;Ability to communicate effectively in English (verbal and written) is essential. &lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before.&lt;br&gt;&lt;br&gt;This is a big step forward.&lt;br&gt;&lt;br&gt;This is work that’ll &lt;strong&gt;move &lt;/strong&gt;you.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;br&gt;#WeAreConvatec&lt;br&gt;&lt;br&gt;&lt;strong&gt;Beware of scams online or from individuals claiming to represent Convatec&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.&lt;br&gt;&lt;br&gt;If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Equal opportunities &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Notice to Agency and Search Firm Representatives&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Already a Convatec employee?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;

R&amp;D Engineer

R&D Engineer

You must have a track record in regulated industries, ISO 13485 knowledge, design control experience, leadership skills, and a relevant degree. Strong communication and problem-solving skills are essential.

You will lead project technical decisions, manage documentation, ensure alignment with stakeholders, oversee team collaboration, and optimize designs with cross-functional engineers.

London

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com We’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – Research and Development Engineering, and you won’t either. The Senior Technical Manager will be part of the R&D Infusion Care business unit. The role is to have a key focus on leading technical development of allocated customer projects, remediation projects, or change projects. This will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. Manager is furthermore to have direct reports of technical resources. Key Responsibilities: * Overseeing technical progress and making technical decisions for allocated projects and acts as lead engineer. * Leading technical documentation development and design control of projects. * Leading design exploration and/or improvements. * Keeping the overview of documentation and dependencies across R&D product portfolio according to the design control processes. * Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions. * Ensuring that all technical aspects of a project including documentations is progressed on time and fulfilling the agreed quality target. * Ensuring escalation of project issues to the NPDL and/or set governance. * Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials. * Handling the day to day work of direct reports. * Building a strong team collaboration and is to ensure sufficient competencies within the team that can support the NPDL’s goals and targets. * Include specific reference to cross functional work and project-based requirements if appropriate. * Ensure abbreviations/acronyms are either not used or clearly explained. Skills & Experience: * Proven track record of managing a technical team in regulated industry. * Good understanding of ISO 13485 and design controls. * Lead Engineering experience. * Practical experience on design control and documentation development for class II+ products. * Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like. * Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations. * Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization. * Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles. * Proven ability to navigate a broad stakeholder environment. * Proven track record of being a technical decision maker. Qualifications/Education: * Bachelor’s Degree in Science or Engineering (or equivalent) is required. * Experience working within the Medical Device Industry or equivalent regulated industry in a Lead Engineering role with a proven track record of delivery excellence. * Experience managing technical teams. * Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly. * Has excellent technical and non-technical communication skill in English, both written and verbally. Team: * The role has the potential to manage a team between 1-7 direct reports over time Travel Requirements: * Up to 10% of international travel Languages: * English (speaking, reading and writing) * Additional languages are welcomed Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it. This is stepping up to a challenge. This is work that’ll move you. Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. Equal opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a Convatec employee? If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.comWe’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – Research and Development Engineering, and you won’t either.The Senior Technical Manager will be part of the R&D Infusion Care business unit. The role is to have a key focus on leading technical development of allocated customer projects, remediation projects, or change projects. This will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. Manager is furthermore to have direct reports of technical resources.Key Responsibilities: * Overseeing technical progress and making technical decisions for allocated projects and acts as lead engineer. * Leading technical documentation development and design control of projects. * Leading design exploration and/or improvements. * Keeping the overview of documentation and dependencies across R&D product portfolio according to the design control processes. * Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions. * Ensuring that all technical aspects of a project including documentations is progressed on time and fulfilling the agreed quality target. * Ensuring escalation of project issues to the NPDL and/or set governance. * Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials. * Handling the day to day work of direct reports. * Building a strong team collaboration and is to ensure sufficient competencies within the team that can support the NPDL’s goals and targets. * Include specific reference to cross functional work and project-based requirements if appropriate. * Ensure abbreviations/acronyms are either not used or clearly explained.         Skills & Experience: * Proven track record of managing a technical team in regulated industry. * Good understanding of ISO 13485 and design controls. * Lead Engineering experience. * Practical experience on design control and documentation development for class II+ products. * Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like. * Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations. * Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization. * Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles. * Proven ability to navigate a broad stakeholder environment. * Proven track record of being a technical decision maker.         Qualifications/Education: * Bachelor’s Degree in Science or Engineering (or equivalent) is required. * Experience working within the Medical Device Industry or equivalent regulated industry in a Lead Engineering role with a proven track record of delivery excellence. * Experience managing technical teams. * Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly. * Has excellent technical and non-technical communication skill in English, both written and verbally.         Team: * The role has the potential to manage a team between 1-7 direct reports over time         Travel Requirements: * Up to 10% of international travel         Languages: * English (speaking, reading and writing) * Additional languages are welcomed         Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.This is stepping up to a challenge.This is work that’ll move you.Beware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Senior Manager – Research and Development Engineering - Convatec

Paddington, England, United Kingdom

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com&lt;br&gt;&lt;br&gt;We’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – Research and Development Engineering, and you won’t either.&lt;br&gt;&lt;br&gt;The Senior Technical Manager will be part of the R&amp;amp;D Infusion Care business unit. The role is to have a key focus on leading technical development of allocated customer projects, remediation projects, or change projects. This will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. Manager is furthermore to have direct reports of technical resources.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Key Responsibilities: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Overseeing technical progress and making technical decisions for allocated projects and acts as lead engineer.&lt;/li&gt;&lt;li&gt;Leading technical documentation development and design control of projects.&lt;/li&gt;&lt;li&gt;Leading design exploration and/or improvements.&lt;/li&gt;&lt;li&gt;Keeping the overview of documentation and dependencies across R&amp;amp;D product portfolio according to the design control processes.&lt;/li&gt;&lt;li&gt;Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions.&lt;/li&gt;&lt;li&gt;Ensuring that all technical aspects of a project including documentations is progressed on time and fulfilling the agreed quality target.&lt;/li&gt;&lt;li&gt;Ensuring escalation of project issues to the NPDL and/or set governance.&lt;/li&gt;&lt;li&gt;Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials.&lt;/li&gt;&lt;li&gt;Handling the day to day work of direct reports.&lt;/li&gt;&lt;li&gt;Building a strong team collaboration and is to ensure sufficient competencies within the team that can support the NPDL’s goals and targets.&lt;/li&gt;&lt;li&gt;Include specific reference to cross functional work and project-based requirements if appropriate.&lt;/li&gt;&lt;li&gt;Ensure abbreviations/acronyms are either not used or clearly explained.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Skills &amp;amp; Experience: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Proven track record of managing a technical team in regulated industry.&lt;/li&gt;&lt;li&gt;Good understanding of ISO 13485 and design controls.&lt;/li&gt;&lt;li&gt;Lead Engineering experience.&lt;/li&gt;&lt;li&gt;Practical experience on design control and documentation development for class II+ products.&lt;/li&gt;&lt;li&gt;Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like.&lt;/li&gt;&lt;li&gt;Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations.&lt;/li&gt;&lt;li&gt;Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization.&lt;/li&gt;&lt;li&gt;Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles.&lt;/li&gt;&lt;li&gt;Proven ability to navigate a broad stakeholder environment.&lt;/li&gt;&lt;li&gt;Proven track record of being a technical decision maker.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications/Education:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor’s Degree in Science or Engineering (or equivalent) is required.&lt;/li&gt;&lt;li&gt;Experience working within the Medical Device Industry or equivalent regulated industry in a Lead Engineering role with a proven track record of delivery excellence.&lt;/li&gt;&lt;li&gt;Experience managing technical teams.&lt;/li&gt;&lt;li&gt;Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly.&lt;/li&gt;&lt;li&gt;Has excellent technical and non-technical communication skill in English, both written and verbally.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Team:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;The role has the potential to manage a team between 1-7 direct reports over time&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Travel Requirements:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Up to 10% of international travel&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Languages:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;English (speaking, reading and writing)&lt;/li&gt;&lt;li&gt;Additional languages are welcomed&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.&lt;br&gt;&lt;br&gt;This is stepping up to a challenge.&lt;br&gt;&lt;br&gt;This is work that’ll &lt;strong&gt;move&lt;/strong&gt; you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Beware of scams online or from individuals claiming to represent Convatec&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.&lt;br&gt;&lt;br&gt;If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Equal opportunities &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Notice to Agency and Search Firm Representatives&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Already a Convatec employee?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;

Senior Manager – Research and Development Engineering

You should have experience in materials, medical device R&D, design control, and statistical sampling. A relevant degree, problem-solving skills, and English proficiency are essential.

You will collaborate across teams on R&D projects, develop test plans, support V&V and regulatory documentation, contribute to risk management, and maintain expertise in scientific advancements.

Science

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com At Convatec, we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us on our journey to #ForeverCaring as a R&D Scientist, and you’ll do the same. Position Overview: Support the execution of key R&D NPD projects/programs through collaboration with various functional groups from concept through to launch. Execute V&V and market support activities to support the launch of new products. Key Responsibilities: * Participate in discussions to resolve technical / scientific challenges to support new product development of * Ostomy Care medical devices. * Translate technical performance requirements into verification and validation test plans. * Facilitate the development of test methods for new performance requirements in conjunction with Laboritories. * Work with cross functional teams to develop and agree upon appropriate test plans for V&V, market support testing. * Support Research and Development project activities within a Design Control Framework in accordance with ISO 13485 & 21CFR820 Quality Systems for Medical Devices. * Write technical documents to support Design Control and regulatory submission. * Contribute to Risk Management activities and other technical assessments. * Generate data to support theories and designs. * Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. * Produce high quality scientific reports to support V&V, regulatory submissions, and market support activities. * Maintain overall expertise by keeping updated on scientific advancements through publications, patents, university / industrial contacts and vendor discussions. * Work with 3rd parties to develop novel research models for V&V and market support activities. * Promote and develop good working relationships within a multidisciplinary team Authority: * Ability to raise PO’s * Author of technical documents * Author of DHF documents Skills & Experience: * Experience of relevant materials and processes desirable (flexible films/fabrics/injection molded parts/electro-mechanical enclosures & assemblies/bonding techniques etc.) * Experience of developing and applying statistical sampling plans during developmentprojects is desirable * Demonstrable industrial experience with knowledge of the application of the design and development and testing of medical devices. * Experience in a R&D medical devices environment and design control is required. * Problem solver: Assess situations & conflicts to identify causes, gather and process relevant information, generate possible solutions, and make recommendations and/or resolve the problem. * Understand ethical behaviour and business practices Qualifications/Education: Degree in Scientific discipline (or equivalent). Principal Contacts & Purpose of Contact: Internal – Lab and V&V teams for test method development, process development for DFM and user centered design team for VOC and usability External – minimal interaction with vendors for prototyping where applicable Travel Requirements Position may involve travel up to 15% of the time, mostly within Europe but overseas travel is expected. Most trips will include overnight travel Languages Speaking: Yes English* Writing/Reading: Yes English* * additional languages as required or nice to have Working Conditions: This is a hybrid role with an expectation to be on site at CTEC Deeside to develop prototypes and run experiments as and when requried Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before. This is a big step forward. This is work that’ll move you. Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. Equal opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a Convatec employee? If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.comAt Convatec, we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us on our journey to #ForeverCaring as a R&D Scientist, and you’ll do the same.Position Overview:Support the execution of key R&D NPD projects/programs through collaboration with various functional groupsfrom concept through to launch. Execute V&V and market support activities to support the launch of new products.Key Responsibilities: * Participate in discussions to resolve technical / scientific challenges to support new product development of * Ostomy Care medical devices. * Translate technical performance requirements into verification and validation test plans. * Facilitate the development of test methods for new performance requirements in conjunction with Laboritories. * Work with cross functional teams to develop and agree upon appropriate test plans for V&V, market support testing. * Support Research and Development project activities within a Design Control Framework in accordance with ISO 13485 & 21CFR820 Quality Systems for Medical Devices. * Write technical documents to support Design Control and regulatory submission. * Contribute to Risk Management activities and other technical assessments. * Generate data to support theories and designs. * Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. * Produce high quality scientific reports to support V&V, regulatory submissions, and market support activities. * Maintain overall expertise by keeping updated on scientific advancements through publications, patents, university / industrial contacts and vendor discussions. * Work with 3rd parties to develop novel research models for V&V and market support activities. * Promote and develop good working relationships within a multidisciplinary team         Authority: * Ability to raise PO’s * Author of technical documents * Author of DHF documents         Skills & Experience: * Experience of relevant materials and processes desirable (flexible films/fabrics/injection molded parts/electro-mechanical enclosures & assemblies/bonding techniques etc.) * Experience of developing and applying statistical sampling plans during developmentprojects is desirable * Demonstrable industrial experience with knowledge of the application of the design and development and testing of medical devices. * Experience in a R&D medical devices environment and design control is required. * Problem solver: Assess situations & conflicts to identify causes, gather and process relevant information, generate possible solutions, and make recommendations and/or resolve the problem. * Understand ethical behaviour and business practices         Qualifications/Education:Degree in Scientific discipline (or equivalent).Principal Contacts & Purpose of Contact:Internal – Lab and V&V teams for test method development, process development for DFM and user centered design team forVOC and usabilityExternal – minimal interaction with vendors for prototyping where applicableTravel RequirementsPosition may involve travel up to 15% of the time, mostly within Europe but overseas travel is expected. Most trips will includeovernight travelLanguagesSpeaking: Yes English*Writing/Reading: Yes English* * additional languages as required or nice to have         Working Conditions:This is a hybrid role with an expectation to be on site at CTEC Deeside to develop prototypes and run experiments as and whenrequriedOur progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before.This is a big step forward.This is work that’ll move you.Beware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Research and Development Scientist - Convatec

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com&lt;br&gt;&lt;br&gt;At Convatec, we’re transforming our business for the better. Better products. Better ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us on our journey to #ForeverCaring as a R&amp;amp;D Scientist, and you’ll do the same.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Position Overview: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Support the execution of key R&amp;amp;D NPD projects/programs through collaboration with various functional groups&lt;br&gt;&lt;br&gt;from concept through to launch. Execute V&amp;amp;V and market support activities to support the launch of new products.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Key Responsibilities: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Participate in discussions to resolve technical / scientific challenges to support new product development of &lt;/li&gt;&lt;li&gt;Ostomy Care medical devices.&lt;/li&gt;&lt;li&gt;Translate technical performance requirements into verification and validation test plans.&lt;/li&gt;&lt;li&gt;Facilitate the development of test methods for new performance requirements in conjunction with Laboritories.&lt;/li&gt;&lt;li&gt;Work with cross functional teams to develop and agree upon appropriate test plans for V&amp;amp;V, market support testing.&lt;/li&gt;&lt;li&gt;Support Research and Development project activities within a Design Control Framework in accordance with ISO 13485 &amp;amp; 21CFR820 Quality Systems for Medical Devices.&lt;/li&gt;&lt;li&gt;Write technical documents to support Design Control and regulatory submission.&lt;/li&gt;&lt;li&gt;Contribute to Risk Management activities and other technical assessments.&lt;/li&gt;&lt;li&gt;Generate data to support theories and designs.&lt;/li&gt;&lt;li&gt;Provide technical input to support the design control process, including contributing to / authoring design history file (DHF) documentation and material specifications. &lt;/li&gt;&lt;li&gt;Produce high quality scientific reports to support V&amp;amp;V, regulatory submissions, and market support activities.&lt;/li&gt;&lt;li&gt;Maintain overall expertise by keeping updated on scientific advancements through publications, patents, university / industrial contacts and vendor discussions.&lt;/li&gt;&lt;li&gt;Work with 3rd parties to develop novel research models for V&amp;amp;V and market support activities.&lt;/li&gt;&lt;li&gt;Promote and develop good working relationships within a multidisciplinary team&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Authority:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Ability to raise PO’s&lt;/li&gt;&lt;li&gt;Author of technical documents&lt;/li&gt;&lt;li&gt;Author of DHF documents&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Skills &amp;amp; Experience: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Experience of relevant materials and processes desirable (flexible films/fabrics/injection molded parts/electro-mechanical enclosures &amp;amp; assemblies/bonding techniques etc.)&lt;/li&gt;&lt;li&gt;Experience of developing and applying statistical sampling plans during developmentprojects is desirable&lt;/li&gt;&lt;li&gt;Demonstrable industrial experience with knowledge of the application of the design and development and testing of medical devices.&lt;/li&gt;&lt;li&gt;Experience in a R&amp;amp;D medical devices environment and design control is required. &lt;/li&gt;&lt;li&gt;Problem solver: Assess situations &amp;amp; conflicts to identify causes, gather and process relevant information, generate possible solutions, and make recommendations and/or resolve the problem.&lt;/li&gt;&lt;li&gt;Understand ethical behaviour and business practices&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications/Education:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Degree in Scientific discipline (or equivalent).&lt;br&gt;&lt;br&gt;&lt;strong&gt;Principal Contacts &amp;amp; Purpose of Contact:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Internal – Lab and V&amp;amp;V teams for test method development, process development for DFM and user centered design team for&lt;br&gt;&lt;br&gt;VOC and usability&lt;br&gt;&lt;br&gt;External – minimal interaction with vendors for prototyping where applicable&lt;br&gt;&lt;br&gt;&lt;strong&gt;Travel Requirements&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Position may involve travel up to 15% of the time, mostly within Europe but overseas travel is expected. Most trips will include&lt;br&gt;&lt;br&gt;overnight travel&lt;br&gt;&lt;br&gt;&lt;strong&gt;Languages&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Speaking: Yes English*&lt;br&gt;&lt;br&gt;Writing/Reading: Yes English*&lt;br&gt;&lt;br&gt;&lt;ul&gt;&lt;li&gt;additional languages as required or nice to have&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Working Conditions:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;This is a hybrid role with an expectation to be on site at CTEC Deeside to develop prototypes and run experiments as and when&lt;br&gt;&lt;br&gt;requried&lt;br&gt;&lt;br&gt;Our progress will give you countless opportunities to move forward too. Seek out new challenges, and you’ll find them. Stretch your thinking, and you’ll find new ways to make an impact. And if you embrace the opportunity to drive your own growth, you could go further, and achieve more, than ever before.&lt;br&gt;&lt;br&gt;This is a big step forward.&lt;br&gt;&lt;br&gt;This is work that’ll &lt;strong&gt;move&lt;/strong&gt; you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Beware of scams online or from individuals claiming to represent Convatec&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.&lt;br&gt;&lt;br&gt;If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Equal opportunities &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Notice to Agency and Search Firm Representatives&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Already a Convatec employee?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;

Research and Development Scientist

You need experience managing teams in regulated industries, R&D collaboration, ISO 13485 knowledge, design control expertise, and strong communication skills. A degree in Science or Engineering is essential.

You will manage external collaborations, oversee project progress, lead technical decisions, ensure documentation quality, and foster team collaboration in product development.

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com We’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – External Research and Development Engineering, and you won’t either. The Senior Manager will be part of the R&D infusion care business unit. The role is to have a key focus on leading and be responsible for all outsourcing activities of technical development of customer projects, remediation projects, or change projects. The role will have a secondary focus on leading internal development projects as well. The external relations and project leadership will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. The manager is furthermore to have direct reports of technical resources. Key Responsibilities: * Maintaining, establishing and managing new and current external collaboration of partners, incl. contractual relationship, negotiation and project management. * Overseeing technical progress and making technical decisions for allocated projects and acting as lead engineer. * Managing pipeline requests for outsourcing activities and ensuring identification of appropriate external partners qualified for the R&D need. * Documentation development and design control of projects. * Leading design exploration and/or improvements. * Keeping the overview of documentation and dependencies across R&D product portfolio according to the design control processes. * Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions. * Ensuring that all technical aspects of a project including documentation is progressed on time and fulfilling the agreed quality target. * Ensuring escalation of project issues to the NPDL and/or set governance. * Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials. * Handling the day to day work of direct reports. * Building a strong team collaboration and ensure sufficient competencies within the team that can support the NPDL’s goals and targets. * Include specific reference to cross functional work and project-based requirements if appropriate. * Ensure abbreviations/acronyms are either not used or clearly explained. Skills & Experience: * Proven track record of managing a technical team in a regulated industry. * Proven track record of managing and successfully collaborating with external partners for R&D projects. * Proven track record of directing R&D teams. * Good understanding of ISO 13485 and design controls. * Lead Engineering experience. * Practical experience on design control and documentation development for class II+ products. * Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like. * Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations. * Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization. * Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles. * Proven ability to navigate a broad stakeholder environment. * Proven track record of being a technical decision maker. Qualifications/Education: * Bachelor’s Degree in Science or Engineering (or equivalent) required. * Experience working within the Medical Device Industry or equivalent Regulated Industry in a Lead Engineering role with a proven track record of delivery excellence. * Experience managing technical teams. * Experience in outsourcing development projects. * Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly. * Has excellent technical and non-technical communication skill in English, both written and verbal. Team: * The role has the potential to manage a team between 1-7 direct reports over time Travel Requirements: * Up to 10% of international travel Languages: * English (speaking, reading and writing) * Additional languages are welcomed Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it. This is stepping up to a challenge. This is work that’ll move you. Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. Equal opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a Convatec employee? If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.comWe’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – External Research and Development Engineering, and you won’t either.The Senior Manager will be part of the R&D infusion care business unit. The role is to have a key focus on leading and be responsible for all outsourcing activities of technical development of customer projects, remediation projects, or change projects. The role will have a secondary focus on leading internal development projects as well. The external relations and project leadership will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. The manager is furthermore to have direct reports of technical resources.Key Responsibilities: * Maintaining, establishing and managing new and current external collaboration of partners, incl. contractual relationship, negotiation and project management. * Overseeing technical progress and making technical decisions for allocated projects and acting as lead engineer. * Managing pipeline requests for outsourcing activities and ensuring identification of appropriate external partners qualified for the R&D need. * Documentation development and design control of projects. * Leading design exploration and/or improvements. * Keeping the overview of documentation and dependencies across R&D product portfolio according to the design control processes. * Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions. * Ensuring that all technical aspects of a project including documentation is progressed on time and fulfilling the agreed quality target. * Ensuring escalation of project issues to the NPDL and/or set governance. * Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials. * Handling the day to day work of direct reports. * Building a strong team collaboration and ensure sufficient competencies within the team that can support the NPDL’s goals and targets. * Include specific reference to cross functional work and project-based requirements if appropriate. * Ensure abbreviations/acronyms are either not used or clearly explained.         Skills & Experience: * Proven track record of managing a technical team in a regulated industry. * Proven track record of managing and successfully collaborating with external partners for R&D projects. * Proven track record of directing R&D teams. * Good understanding of ISO 13485 and design controls. * Lead Engineering experience. * Practical experience on design control and documentation development for class II+ products. * Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like. * Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations. * Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization. * Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles. * Proven ability to navigate a broad stakeholder environment. * Proven track record of being a technical decision maker.         Qualifications/Education: * Bachelor’s Degree in Science or Engineering (or equivalent) required. * Experience working within the Medical Device Industry or equivalent Regulated Industry in a Lead Engineering role with a proven track record of delivery excellence. * Experience managing technical teams. * Experience in outsourcing development projects. * Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly. * Has excellent technical and non-technical communication skill in English, both written and verbal.         Team: * The role has the potential to manage a team between 1-7 direct reports over time         Travel Requirements: * Up to 10% of international travel         Languages: * English (speaking, reading and writing) * Additional languages are welcomed         Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.This is stepping up to a challenge.This is work that’ll move you.Beware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Senior Manager – External Research and Development Engineering - Convatec

Pioneering trusted medical solutions to improve the lives we touch: Unomedical s.r.o. is a member of Convatec which is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com&lt;br&gt;&lt;br&gt;We’re a business that never stands still. Join us on our journey to #ForeverCaring as a Senior Manager – External Research and Development Engineering, and you won’t either.&lt;br&gt;&lt;br&gt;The Senior Manager will be part of the R&amp;amp;D infusion care business unit. The role is to have a key focus on leading and be responsible for all outsourcing activities of technical development of customer projects, remediation projects, or change projects. The role will have a secondary focus on leading internal development projects as well. The external relations and project leadership will be done in close collaboration with the NPDL. The role‘s objective is to deliver on a subset of the NPDL’s goals and targets. The manager is furthermore to have direct reports of technical resources.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Key Responsibilities: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Maintaining, establishing and managing new and current external collaboration of partners, incl. contractual relationship, negotiation and project management.&lt;/li&gt;&lt;li&gt;Overseeing technical progress and making technical decisions for allocated projects and acting as lead engineer.&lt;/li&gt;&lt;li&gt;Managing pipeline requests for outsourcing activities and ensuring identification of appropriate external partners qualified for the R&amp;amp;D need.&lt;/li&gt;&lt;li&gt;Documentation development and design control of projects.&lt;/li&gt;&lt;li&gt;Leading design exploration and/or improvements.&lt;/li&gt;&lt;li&gt;Keeping the overview of documentation and dependencies across R&amp;amp;D product portfolio according to the design control processes.&lt;/li&gt;&lt;li&gt;Ensuring that projects are aligned with the NPDL and key stakeholders on critical decisions.&lt;/li&gt;&lt;li&gt;Ensuring that all technical aspects of a project including documentation is progressed on time and fulfilling the agreed quality target.&lt;/li&gt;&lt;li&gt;Ensuring escalation of project issues to the NPDL and/or set governance.&lt;/li&gt;&lt;li&gt;Work together with cross functional product development engineers to optimize designs for manufacturability, build prototypes and conduct proof-of-principle, and pilot-scale manufacturing trials.&lt;/li&gt;&lt;li&gt;Handling the day to day work of direct reports.&lt;/li&gt;&lt;li&gt;Building a strong team collaboration and ensure sufficient competencies within the team that can support the NPDL’s goals and targets.&lt;/li&gt;&lt;li&gt;Include specific reference to cross functional work and project-based requirements if appropriate.&lt;/li&gt;&lt;li&gt;Ensure abbreviations/acronyms are either not used or clearly explained.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Skills &amp;amp; Experience: &lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Proven track record of managing a technical team in a regulated industry.&lt;/li&gt;&lt;li&gt;Proven track record of managing and successfully collaborating with external partners for R&amp;amp;D projects.&lt;/li&gt;&lt;li&gt;Proven track record of directing R&amp;amp;D teams.&lt;/li&gt;&lt;li&gt;Good understanding of ISO 13485 and design controls.&lt;/li&gt;&lt;li&gt;Lead Engineering experience.&lt;/li&gt;&lt;li&gt;Practical experience on design control and documentation development for class II+ products.&lt;/li&gt;&lt;li&gt;Experience in applying in-depth process knowledge to help inform design and process FMEAs, set realistic tolerances, devise sampling plans, and the like.&lt;/li&gt;&lt;li&gt;Track record of participating in product development projects needing Design for Manufacture and Design for Assembly considerations.&lt;/li&gt;&lt;li&gt;Proven track record of applying modern engineering theory, critical thinking, and statistical analysis to structure problem solving and process design optimization.&lt;/li&gt;&lt;li&gt;Good understanding for mechanical engineering disciplines such as tolerance analysis, molding, CAD drawings, requirement engineering, design verification and validation principles.&lt;/li&gt;&lt;li&gt;Proven ability to navigate a broad stakeholder environment.&lt;/li&gt;&lt;li&gt;Proven track record of being a technical decision maker.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Qualifications/Education:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Bachelor’s Degree in Science or Engineering (or equivalent) required.&lt;/li&gt;&lt;li&gt;Experience working within the Medical Device Industry or equivalent Regulated Industry in a Lead Engineering role with a proven track record of delivery excellence.&lt;/li&gt;&lt;li&gt;Experience managing technical teams.&lt;/li&gt;&lt;li&gt;Experience in outsourcing development projects.&lt;/li&gt;&lt;li&gt;Ability to understand business and operational objectives, and to prioritize high volume and complex workloads accordingly.&lt;/li&gt;&lt;li&gt;Has excellent technical and non-technical communication skill in English, both written and verbal.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Team:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;The role has the potential to manage a team between 1-7 direct reports over time&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Travel Requirements:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Up to 10% of international travel&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Languages:&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;English (speaking, reading and writing)&lt;/li&gt;&lt;li&gt;Additional languages are welcomed&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Our ambitions will bring the very best out in you. You’ll be pushed to aim higher and really own your work. You’ll be encouraged and supported to make things happen, too. It can be challenging. But, as the progress you make will help improve the lives of millions, it’ll be worth it.&lt;br&gt;&lt;br&gt;This is stepping up to a challenge.&lt;br&gt;&lt;br&gt;This is work that’ll &lt;strong&gt;move&lt;/strong&gt; you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Beware of scams online or from individuals claiming to represent Convatec&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.&lt;br&gt;&lt;br&gt;If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Equal opportunities &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Notice to Agency and Search Firm Representatives&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Already a Convatec employee?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;

Senior Manager – External Research and Development Engineering

You have a degree in business or similar, experience in sales leadership, medical device knowledge, excellent communication skills, and are willing to travel. Proficiency in English is essential.

You will drive commercial activities, develop strategies and objectives, build customer relationships, and collaborate with teams to enhance business growth and address customer needs effectively.

Sales & Business Development

Healthcare

Munich

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC). To learn more about Convatec, please visit http://www.convatecgroup.com At ConvaTec, we’re transforming our business for the better. Better products. etter ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us and you’ll do the same. We’re looking for a talented Regional Commercial Manager for our Neria Business for the Central European Region. With responsibility for a diverse and mature team of 4 people across Europe, you will play a central role for our Commercial Business in Infusion Care. OUR PROMISE * the opportunity to work independently in a dynamic, informal and international environment * a unique and “forever caring” company culture * market leading and innovative product offering * the possibility to work remote in a hybrid model * exceptional benefits and a professional onboarding/training Your Key Responsibilities * Building and implementing the Regional strategy aligned with our Global strategy, setting the team up for success and ensuring the delivery of objectives through a high performing team. * Drive all commercial activities within Infusion Care (IC) in Central Europe (DACH; BNL; DK; CEE). * Plan and implement successful business plans and enable business growth. * Define commercial objectives for the Region (Budgets, Targets and Objectives KPI’s, CRM metrics). * Create a shared vision and strong team ethos and ensure IC Central Europe Region team are fully motivated to succeed . * Develop the team to enable them to communicate both clinical and value-based conversations with clinical and commercial stakeholders. * Build relationships with key customers, decision makers, distributors and wholesalers to understand end user needs, demand, forecasts and inventory levels. * Use market insights to support team with account segmentation and prioritisation, collaborating closely with Sales Force Effectivness managers. * Gather information from KOLs as to how they are using our technologies & feed this information back to marketing and sales colleagues to help develop marketing materials and commercial strategies. * Work with cross functional Teams to ensure that all aspects of customer issues are addressed and resolved effectively and professionally (Business reviews, pricing adjustments, etc.). * Collaborate with global sales and marketing colleagues to create clear and concise value propositions. * Coordinate sales and marketing campaigns with customer and IC marketing. * Engage with B2B and B2C customers through regular consultations and face to face business meetings. YOUR PROFILE * Master’s or Bachelor’s degree in business, marketing, economic or similar, alternatively an equivalent education combined with relevant experience. * You are an experienced first line sales manager with demonstrable evidence of leading a team to high levels of performance * Demonstrable previous sales success at an individual level. * You are highly motivated, determined with a strong interpersonal skillset and the ability to lead. * Ability to negotiate and manage through influence. * Excellent communication and presentation skills. * Ability to manage multiple projects and adapt priorities according to business and strategic needs. * A clear drive and focus on what is important and what needs to be done to enable success. * Profound understanding of/and experience with the medical device industry * Understanding of National health systems in the Region is highly preferable. * You have interpersonal skills to enable building trusted relationships with B2B customers. * Experience in working in a global organization. * Profound English skills both written and spoken is a requirement. * You live near our Copenhagen office or our Munich office is a peference. * We would expect you to be comfortable to be present in an office site on a regular base as well as with up to 30 travel days annualy Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet. This is stepping outside of your comfort zone. This is work that’ll move you. Beware of scams online or from individuals claiming to represent Convatec A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address. If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com. Equal opportunities Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law. Notice to Agency and Search Firm Representatives Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you. Already a Convatec employee? If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC).To learn more about Convatec, please visit http://www.convatecgroup.comAt ConvaTec, we’re transforming our business for the better. Better products. etter ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us and you’ll do the same.We’re looking for a talented Regional Commercial Manager for our Neria Business for the Central European Region. With responsibility for a diverse and mature team of 4 people across Europe, you will play a central role for our Commercial Business in Infusion Care.OUR PROMISE * the opportunity to work independently in a dynamic, informal and international environment * a unique and “forever caring” company culture * market leading and innovative product offering * the possibility to work remote in a hybrid model * exceptional benefits and a professional onboarding/training         Your Key Responsibilities * Building and implementing the Regional strategy aligned with our Global strategy, setting the team up for success and ensuring the delivery of objectives through a high performing team. * Drive all commercial activities within Infusion Care (IC) in Central Europe (DACH; BNL; DK; CEE). * Plan and implement successful business plans and enable business growth. * Define commercial objectives for the Region (Budgets, Targets and Objectives KPI’s, CRM metrics). * Create a shared vision and strong team ethos and ensure IC Central Europe Region team are fully motivated to succeed . * Develop the team to enable them to communicate both clinical and value-based conversations with clinical and commercial stakeholders. * Build relationships with key customers, decision makers, distributors and wholesalers to understand end user needs, demand, forecasts and inventory levels. * Use market insights to support team with account segmentation and prioritisation, collaborating closely with Sales Force Effectivness managers. * Gather information from KOLs as to how they are using our technologies & feed this information back to marketing and sales colleagues to help develop marketing materials and commercial strategies. * Work with cross functional Teams to ensure that all aspects of customer issues are addressed and resolved effectively and professionally (Business reviews, pricing adjustments, etc.). * Collaborate with global sales and marketing colleagues to create clear and concise value propositions. * Coordinate sales and marketing campaigns with customer and IC marketing. * Engage with B2B and B2C customers through regular consultations and face to face business meetings.         YOUR PROFILE * Master’s or Bachelor’s degree in business, marketing, economic or similar, alternatively an equivalent education combined with relevant experience. * You are an experienced first line sales manager with demonstrable evidence of leading a team to high levels of performance * Demonstrable previous sales success at an individual level. * You are highly motivated, determined with a strong interpersonal skillset and the ability to lead. * Ability to negotiate and manage through influence. * Excellent communication and presentation skills. * Ability to manage multiple projects and adapt priorities according to business and strategic needs. * A clear drive and focus on what is important and what needs to be done to enable success. * Profound understanding of/and experience with the medical device industry * Understanding of National health systems in the Region is highly preferable. * You have interpersonal skills to enable building trusted relationships with B2B customers. * Experience in working in a global organization. * Profound English skills both written and spoken is a requirement. * You live near our Copenhagen office or our Munich office is a peference. * We would expect you to be comfortable to be present in an office site on a regular base as well as with up to 30 travel days annualy         Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet.This is stepping outside of your comfort zone.This is work that’ll move you.Beware of scams online or from individuals claiming to represent ConvatecA formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.Equal opportunitiesConvatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.Notice to Agency and Search Firm RepresentativesConvatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.Already a Convatec employee?If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!

Regional Commercial Manager – Infusion Care (Central Europe) - Convatec

Pioneering trusted medical solutions to improve the lives we touch: Convatec is a global medical products and technologies company, focused on solutions for the management of chronic conditions, with leading positions in advanced wound care, ostomy care, continence care, and infusion care. With around 10,000 colleagues, we provide our products and services in almost 100 countries, united by a promise to be forever caring. Our solutions provide a range of benefits, from infection prevention and protection of at-risk skin, to improved patient outcomes and reduced care costs. Convatec’s revenues in 2023 were over $2 billion. The company is a constituent of the FTSE 100 Index (LSE:CTEC).&lt;br&gt;&lt;br&gt;To learn more about Convatec, please visit http://www.convatecgroup.com&lt;br&gt;&lt;br&gt;At ConvaTec, we’re transforming our business for the better. Better products. etter ways of working. And better ways of delivering for our customers and each other. We’re aiming for nothing short of excellence. Join us and you’ll do the same.&lt;br&gt;&lt;br&gt;We’re looking for a talented &lt;strong&gt;Regional Commercial Manager &lt;/strong&gt;for our Neria Business for the Central European Region. With responsibility for a diverse and mature team of 4 people across Europe, you will play a central role for our Commercial Business in Infusion Care.&lt;br&gt;&lt;br&gt;&lt;strong&gt;OUR PROMISE&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;the opportunity to work independently in a dynamic, informal and international environment&lt;/li&gt;&lt;li&gt;a unique and “forever caring” company culture&lt;/li&gt;&lt;li&gt;market leading and innovative product offering&lt;/li&gt;&lt;li&gt;the possibility to work remote in a hybrid model&lt;/li&gt;&lt;li&gt;exceptional benefits and a professional onboarding/training&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;Your Key Responsibilities&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Building and implementing the Regional strategy aligned with our Global strategy, setting the team up for success and ensuring the delivery of objectives through a high performing team.&lt;/li&gt;&lt;li&gt;Drive all commercial activities within Infusion Care (IC) in Central Europe (DACH; BNL; DK; CEE).&lt;/li&gt;&lt;li&gt;Plan and implement successful business plans and enable business growth.&lt;/li&gt;&lt;li&gt;Define commercial objectives for the Region (Budgets, Targets and Objectives KPI’s, CRM metrics).&lt;/li&gt;&lt;li&gt;Create a shared vision and strong team ethos and ensure IC Central Europe Region team are fully motivated to succeed .&lt;/li&gt;&lt;li&gt;Develop the team to enable them to communicate both clinical and value-based conversations with clinical and commercial stakeholders.&lt;/li&gt;&lt;li&gt;Build relationships with key customers, decision makers, distributors and wholesalers to understand end user needs, demand, forecasts and inventory levels.&lt;/li&gt;&lt;li&gt;Use market insights to support team with account segmentation and prioritisation, collaborating closely with Sales Force Effectivness managers.&lt;/li&gt;&lt;li&gt;Gather information from KOLs as to how they are using our technologies &amp;amp; feed this information back to marketing and sales colleagues to help develop marketing materials and commercial strategies.&lt;/li&gt;&lt;li&gt;Work with cross functional Teams to ensure that all aspects of customer issues are addressed and resolved effectively and professionally (Business reviews, pricing adjustments, etc.).&lt;/li&gt;&lt;li&gt;Collaborate with global sales and marketing colleagues to create clear and concise value propositions.&lt;/li&gt;&lt;li&gt;Coordinate sales and marketing campaigns with customer and IC marketing.&lt;/li&gt;&lt;li&gt;Engage with B2B and B2C customers through regular consultations and face to face business meetings.&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;&lt;strong&gt;YOUR PROFILE&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;ul&gt;&lt;li&gt;Master’s or Bachelor’s degree in business, marketing, economic or similar, alternatively an equivalent education combined with relevant experience.&lt;/li&gt;&lt;li&gt;You are an experienced first line sales manager with demonstrable evidence of leading a team to high levels of performance&lt;/li&gt;&lt;li&gt;Demonstrable previous sales success at an individual level.&lt;/li&gt;&lt;li&gt;You are highly motivated, determined with a strong interpersonal skillset and the ability to lead.&lt;/li&gt;&lt;li&gt;Ability to negotiate and manage through influence.&lt;/li&gt;&lt;li&gt;Excellent communication and presentation skills.&lt;/li&gt;&lt;li&gt;Ability to manage multiple projects and adapt priorities according to business and strategic needs.&lt;/li&gt;&lt;li&gt;A clear drive and focus on what is important and what needs to be done to enable success.&lt;/li&gt;&lt;li&gt;Profound understanding of/and experience with the medical device industry&lt;/li&gt;&lt;li&gt;Understanding of National health systems in the Region is highly preferable.&lt;/li&gt;&lt;li&gt;You have interpersonal skills to enable building trusted relationships with B2B customers.&lt;/li&gt;&lt;li&gt;Experience in working in a global organization.&lt;/li&gt;&lt;li&gt;Profound English skills both written and spoken is a requirement.&lt;/li&gt;&lt;li&gt;You live near our Copenhagen office or our Munich office is a peference.&lt;/li&gt;&lt;li&gt;We would expect you to be comfortable to be present in an office site on a regular base as well as with up to 30 travel days annualy&lt;br&gt;&lt;br&gt;&lt;br&gt;&lt;/li&gt;&lt;/ul&gt;Our transformation will change your career. For good. You’ll be pushed to think bigger and aim for excellence. Your ideas will be heard, and you’ll be supported to bring them to life. There’ll be challenges. But, stretch yourself and embrace the opportunities, and you could make your biggest impact yet.&lt;br&gt;&lt;br&gt;This is stepping outside of your comfort zone.&lt;br&gt;&lt;br&gt;&lt;strong&gt;This is work that’ll move you.&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;Beware of scams online or from individuals claiming to represent Convatec&lt;br&gt;&lt;br&gt;&lt;/strong&gt;A formal recruitment process is required for all our opportunities prior to any offer of employment. This will include an interview confirmed by an official Convatec email address.&lt;br&gt;&lt;br&gt;If you receive a suspicious approach over social media, text message, email or phone call about recruitment at Convatec, do not disclose any personal information or pay any fees whatsoever. If you’re unsure, please contact us at careers@Convatec.com.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Equal opportunities &lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec provides equal employment opportunities for all current employees and applicants for employment. This policy means that no one will be discriminated against because of race, religion, creed, color, national origin, nationality, citizenship, ancestry, sex, age, marital status, physical or mental disability, affectional or sexual orientation, gender identity, military or veteran status, genetic predisposing characteristics or any other basis prohibited by law.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Notice to Agency and Search Firm Representatives&lt;br&gt;&lt;br&gt;&lt;/strong&gt;Convatec is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Convatec employee by a third party agency and/or search firm without a valid written and signed search agreement, will become the sole property of Convatec. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.&lt;br&gt;&lt;br&gt;&lt;strong&gt;Already a Convatec employee?&lt;br&gt;&lt;br&gt;&lt;/strong&gt;&lt;strong&gt;If you are an active employee at Convatec, please do not apply here. Go to the Career Worklet on your Workday home page and View "Convatec Internal Career Site - Find Jobs". Thank you!&lt;br&gt;&lt;br&gt;&lt;/strong&gt;

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