Large

Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $40 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, increasing productivity in their laboratories, improving patient health through diagnostics or the development and manufacture of life-changing therapies, we are here to support them. Our global team delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services, Patheon and PPD.

Science & Healthcare

Thermo Fisher Scientific

<div>
 Work Schedule Other
 
 Environmental Conditions Office
 
 Job Description
 
 <h2 class="jobSectionHeader"> Job Title: Creative Design Technician</h2>
 Location: Horsham- hybrid
 <h2 class="jobSectionHeader"> Position Summary:</h2>
 
 As part of the Engineering function, the Creative Design Technician will provide the required CAD (Computer Aided Design) technical support and drawings to our Client Services, Packaging Operations, Distribution and Sales Departments.
 This could involve 3D concept designs for quotations, tool designs, packaging and kit design, manufacturing drawings for suppliers, and producing 3D visual and instructional drawings for operations.
 Ability to turn designs and drawings into animations, for clients, sales and marketing. Focus on practical process improvement &amp; innovation in conjunction with the engineering team. Day to day project management in technical drawing completion.
 
 <h2 class="jobSectionHeader"> Responsibilities:</h2>
 
 The role carries responsibility for the support in the engineering department with "innovative" technology to support the Manufacturing process development.
 <ul>
 <li> Packaging and tool design, sample ordering and project management through to completion.</li>
 <li> Ensuring the design of printed/non-printed packaging components are fit for purpose, meet client expectation, whilst providing maximum efficiency &amp; regulatory requirements.</li>
 <li> Keeping up-to-date with applicable clinical regulations and technical advances within a GxP environment.</li>
 <li> Collaborate at a site level and globally with other ThermoFisher colleagues. Working as one team to improve processes.</li>
 <li> Assist with department and inter-departmental cross training in standard process.</li>
 <li> Provide technical and visual communications across the company as requested (Animations, presentations, banners and posters).</li>
 <li> Maintain technical knowledge through continuous professional development.</li>
 <li> Occasional requirement to present design concepts to clients, both internal and external.</li>
 </ul>
 
 <h2 class="jobSectionHeader"> Minimum Requirements/Qualifications: </h2>
 
 The ideal candidate will have a background within engineering in the pharmaceutical industry though other industries considered.
 <ul>
 <li> Relevant experience of GxP and clinical trial packaging.</li>
 <li> Able to analyse problems and define solutions.</li>
 <li> Ability to produce innovative design solutions.</li>
 <li> Able to work in a busy and lively environment to support others within the team.</li>
 </ul>
 <h2 class="jobSectionHeader"> Job Specific Software Proficiencies:</h2>
 <ul>
 <li> Autodesk Inventor 3D (certified user).</li>
 <li> AutoCAD LT.</li>
 <li> Autodesk Vault Professional.</li>
 <li> 3DS Max.</li>
 <li> Adobe Creative Suite: Illustrator, Photoshop, Acrobat.</li>
 <li> General Microsoft proficiencies; Excel, Word, Powerpoint.</li>
 </ul>
 
 Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 
 <h2 class="jobSectionHeader"> Apply today! http://jobs.thermofisher.com</h2>
 
 Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
</div>


 Work Schedule Other
 
  Environmental Conditions Office
 
  Job Description
 
  Job Title: Creative Design Technician
  Location: Horsham- hybrid
  Position Summary:
 
  As part of the Engineering function, the Creative Design Technician will provide the required CAD (Computer Aided Design) technical support and drawings to our Client Services, Packaging Operations, Distribution and Sales Departments.
  This could involve 3D concept designs for quotations, tool designs, packaging and kit design, manufacturing drawings for suppliers, and producing 3D visual and instructional drawings for operations.
  Ability to turn designs and drawings into animations, for clients, sales and marketing. Focus on practical process improvement & innovation in conjunction with the engineering team. Day to day project management in technical drawing completion.
 
  Responsibilities:
 
  The role carries responsibility for the support in the engineering department with "innovative" technology to support the Manufacturing process development.
 
   Packaging and tool design, sample ordering and project management through to completion.
   Ensuring the design of printed/non-printed packaging components are fit for purpose, meet client expectation, whilst providing maximum efficiency & regulatory requirements.
   Keeping up-to-date with applicable clinical regulations and technical advances within a GxP environment.
   Collaborate at a site level and globally with other ThermoFisher colleagues. Working as one team to improve processes.
   Assist with department and inter-departmental cross training in standard process.
   Provide technical and visual communications across the company as requested (Animations, presentations, banners and posters).
   Maintain technical knowledge through continuous professional development.
   Occasional requirement to present design concepts to clients, both internal and external.
 
 
  Minimum Requirements/Qualifications: 
 
 The ideal candidate will have a background within engineering in the pharmaceutical industry though other industries considered.
 
   Relevant experience of GxP and clinical trial packaging.
   Able to analyse problems and define solutions.
   Ability to produce innovative design solutions.
   Able to work in a busy and lively environment to support others within the team.
 
  Job Specific Software Proficiencies:
 
   Autodesk Inventor 3D (certified user).
   AutoCAD LT.
   Autodesk Vault Professional.
   3DS Max.
   Adobe Creative Suite: Illustrator, Photoshop, Acrobat.
   General Microsoft proficiencies; Excel, Word, Powerpoint.
 
 
  Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 
  Apply today! http://jobs.thermofisher.com
 
  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.


Creative Design Technician - Thermo Fisher Scientific

Creative Design Technician

You must have relevant scientific experience, strong analytical skills, familiarity with manufacturing processes, and a passion for innovating in the life sciences industry.

You will conduct experiments, analyze data, optimize manufacturing processes, and collaborate with teams to ensure product quality and efficiency in bioproduction.

Saint Louis

<div>
 Work Schedule Standard (Mon-Fri)
 
 Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
 
 Job Description
 
 How will you make an impact?
 We are searching for a Process Engineer 1 with education in biopharmaceutical processing, or a related field. This member of our team uses their foundational knowledge in general scientific and engineering principles to provide technological input in the scale up and validation of manufacturing processes. A Process Engineer 1 supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will assist in defining and shaping Thermo Fisher Scientific’s own technology programs. This role will collaborate internally with technicians in the Operations department, Quality Assurance, fellow Engineers, and scientists in Process Development. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.
 Standard Job Duties
 <ul>
 <li> Collaborate with the process development to assess and learn new methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, and purification.</li>
 <li> Demonstrate initiative and attention to detail and an eagerness to learn new systems and technologies.</li>
 <li> Attend Internal and Customer meetings guided by supervision, may occasionally present data.</li>
 <li> Manages internal projects and tasks on time. Actively identify error proofing opportunities and participate in driving engineering initiatives to improve practices and procedures.</li>
 <li> Provide scientific input for GMP minor deviations.</li>
 <li> Support mock and quality audits </li>
 <li> Participate in changes to equipment and process design.</li>
 <li> Draft Manufacturing Batch Records, Performance Qualifications, Process Validation protocols, Process flow diagrams, Automation methods, and Bill of Materials, ensuring the process is technically accurate and designed for Manufacturing.</li>
 <li> Performs daily data monitoring and data collection. Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility.</li>
 <li> Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers.</li>
 </ul>
 How will you get here?
 Education
 <ul>
 <li> Bachelor’s degree required in a scientific field, preferably an engineering field</li>
 </ul>
 Experience
 <ul>
 <li> Follow Environmental, Health and Safety policies and procedures and ensure a safe and healthy workplace environment.</li>
 <li> Ability to self-motivate, prioritize work and time.</li>
 <li> Demonstrates a foundation in general scientific practices, principles, and concepts.</li>
 <li> Writes and communicates effectively.</li>
 <li> Ability to work both independently and as part of a team.</li>
 <li> Knowledge of current Good Manufacturing Practices and US/EU regulations.</li>
 <li> Fundamental knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus.</li>
 <li> Proficient in Microsoft Word and Excel.</li>
 <li> Ability to stand for prolonged periods of time and gown into manufacturing areas.</li>
 </ul>
 Relocation Benefits
 This position does not offer relocation benefits.
 
 Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 Apply today! http://jobs.thermofisher.com
 Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
</div>


 Work Schedule Standard (Mon-Fri)
 
  Environmental Conditions Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Cleanroom: no hair products, jewelry, makeup, nail polish, perfume, exposed piercings, facial hair etc... allowed, Office, Some degree of PPE (Personal Protective Equipment) required (safety glasses, gowning, gloves, lab coat, ear plugs etc.)
 
  Job Description
 
  How will you make an impact?
  We are searching for a Process Engineer 1 with education in biopharmaceutical processing, or a related field. This member of our team uses their foundational knowledge in general scientific and engineering principles to provide technological input in the scale up and validation of manufacturing processes. A Process Engineer 1 supports the Process Engineering team as technical owners of customer programs in a manufacturing environment and will assist in defining and shaping Thermo Fisher Scientific’s own technology programs. This role will collaborate internally with technicians in the Operations department, Quality Assurance, fellow Engineers, and scientists in Process Development. These activities are conducted in projects and involve teamwork with experts across functional groups to ensure project success.
  Standard Job Duties
 
   Collaborate with the process development to assess and learn new methodologies for conducting unit operations at the manufacturing scale including cell culture, harvest, and purification.
   Demonstrate initiative and attention to detail and an eagerness to learn new systems and technologies.
   Attend Internal and Customer meetings guided by supervision, may occasionally present data.
   Manages internal projects and tasks on time. Actively identify error proofing opportunities and participate in driving engineering initiatives to improve practices and procedures.
   Provide scientific input for GMP minor deviations.
   Support mock and quality audits 
   Participate in changes to equipment and process design.
   Draft Manufacturing Batch Records, Performance Qualifications, Process Validation protocols, Process flow diagrams, Automation methods, and Bill of Materials, ensuring the process is technically accurate and designed for Manufacturing.
   Performs daily data monitoring and data collection. Troubleshoot technical challenges on the manufacturing floor as needed for a 24/7 manufacturing facility.
   Support our MSAT team with additional tasks to improve the site, ensure patient safety, and deliver for our customers.
 
  How will you get here?
  Education
 
   Bachelor’s degree required in a scientific field, preferably an engineering field
 
  Experience
 
   Follow Environmental, Health and Safety policies and procedures and ensure a safe and healthy workplace environment.
   Ability to self-motivate, prioritize work and time.
   Demonstrates a foundation in general scientific practices, principles, and concepts.
   Writes and communicates effectively.
   Ability to work both independently and as part of a team.
   Knowledge of current Good Manufacturing Practices and US/EU regulations.
   Fundamental knowledge of statistical methods used for Pharmaceutical Process Analysis is a plus.
   Proficient in Microsoft Word and Excel.
   Ability to stand for prolonged periods of time and gown into manufacturing areas.
 
  Relocation Benefits
  This position does not offer relocation benefits.
 
  Our Mission is to enable our customers to make the world healthier, cleaner, and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation, and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation, and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
  Apply today! http://jobs.thermofisher.com
  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.


Scientist I, Manufacturing Sciences - Thermo Fisher Scientific

Scientist I, Manufacturing Sciences

You should have experience in software testing, strong analytical skills, knowledge of QA methodologies, and familiarity with automated testing tools. Effective communication and teamwork skills are essential.

You will design and execute test plans, identify and document defects, perform regression testing, collaborate with development teams, and ensure software quality meets standards.

Tewksbury

<div>
 Work Schedule Standard (Mon-Fri)
 
 Environmental Conditions Office
 
 Job Description
 
 Do you have a passion for innovative ideas and ground-breaking discoveries? With over $1 billion invested annually in R&amp;D, at Thermo Fisher Scientific you’ll help solve some of the world’s toughest challenges, from giving cancer patients hope, ensuring safe drinking water and helping law enforcement tackle cases through forensics. We empower our teams to put science into meaningful action and give our R&amp;D colleagues the autonomy, resources and tools they need to take science a step beyond.
 
 Tewksbury MA/Chemical Analysis Division/ Production Process &amp; Analytics Business Unit
 The Chemical Analysis business provides a broad mix of analytical instruments and services to a diverse range of end user markets including Safety &amp; Security, Environmental, Food Safety, Life Sciences, Medical, Energy, and Minerals and Mining. Its instruments are deployed globally in the field and on the line, in dynamic environments where customers put a premium on quality, reliability and ease of use. The Chemical Analysis business operates within a global footprint with more than 2,000 colleagues, delivering product solutions to customers that allow for confident, on-the-spot decision making.
 <h2 class="jobSectionHeader"> How you will make an impact:</h2>
 As a Software Quality Assurance (SQA) Engineer III the extensiveness of your role will allow you to play a pivotal part in working on and the qualification of ground-breaking technology for devices that make the world a healthier, cleaner, and safer place. In this role you will have a chance to work with other software, electrical, and mechanical engineers as well as scientists to qualify something from inception to first customer shipment. This role provides the opportunity to grow within the Software Quality Assurance team and across the Thermo Fisher organization. Benefits include 401k, healthcare and vision coverage, employee assistance program, 24/7 virtual doctor visits, back up children and eldercare, and more!
 <h2 class="jobSectionHeader"> What you will do:</h2>
 <ul>
 <li> Experience with software validation on embedded devices (desired)</li>
 <li> Ability to work with multi-disciplined, global teams.</li>
 <li> Strong knowledge in understanding system functional requirements, test case development, test execution, defect reporting and verification.</li>
 <li> Experience within agile software development lifecycle processes</li>
 <li> Tools: Jira, Confluence and Xray.</li>
 </ul>
 <h2 class="jobSectionHeader"> How you will get here:</h2>
 Education
 <ul>
 <li> BS in Computer Science, Engineering or Mathematics and 2 – 5 years of related experience.</li>
 </ul>
 <h2 class="jobSectionHeader"> Knowledge, Skills, Abilities</h2>
 <ul>
 <li> Experience with software validation on embedded devices</li>
 <li> Ability to work with multi-disciplined, global teams</li>
 <li> Strong knowledge in understanding system functional requirements, test case development, test execution, defect reporting and verification.</li>
 <li> Experience within agile software development lifecycle processes</li>
 <li> Tools: Jira, Confluence and XRay</li>
 </ul>
 
 Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 <h2 class="jobSectionHeader"> Apply today! http://jobs.thermofisher.com</h2>
 Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
 <h2 class="jobSectionHeader"> Accessibility/Disability Access</h2>
 Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
 <ul>
 <li> This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.</li>
 </ul>
</div>


 Work Schedule Standard (Mon-Fri)
 
  Environmental Conditions Office
 
  Job Description
 
  Do you have a passion for innovative ideas and ground-breaking discoveries? With over $1 billion invested annually in R&D, at Thermo Fisher Scientific you’ll help solve some of the world’s toughest challenges, from giving cancer patients hope, ensuring safe drinking water and helping law enforcement tackle cases through forensics. We empower our teams to put science into meaningful action and give our R&D colleagues the autonomy, resources and tools they need to take science a step beyond.
 
  Tewksbury MA/Chemical Analysis Division/ Production Process & Analytics Business Unit
  The Chemical Analysis business provides a broad mix of analytical instruments and services to a diverse range of end user markets including Safety & Security, Environmental, Food Safety, Life Sciences, Medical, Energy, and Minerals and Mining. Its instruments are deployed globally in the field and on the line, in dynamic environments where customers put a premium on quality, reliability and ease of use. The Chemical Analysis business operates within a global footprint with more than 2,000 colleagues, delivering product solutions to customers that allow for confident, on-the-spot decision making.
  How you will make an impact:
  As a Software Quality Assurance (SQA) Engineer III the extensiveness of your role will allow you to play a pivotal part in working on and the qualification of ground-breaking technology for devices that make the world a healthier, cleaner, and safer place. In this role you will have a chance to work with other software, electrical, and mechanical engineers as well as scientists to qualify something from inception to first customer shipment. This role provides the opportunity to grow within the Software Quality Assurance team and across the Thermo Fisher organization. Benefits include 401k, healthcare and vision coverage, employee assistance program, 24/7 virtual doctor visits, back up children and eldercare, and more!
  What you will do:
 
   Experience with software validation on embedded devices (desired)
   Ability to work with multi-disciplined, global teams.
   Strong knowledge in understanding system functional requirements, test case development, test execution, defect reporting and verification.
   Experience within agile software development lifecycle processes
   Tools: Jira, Confluence and Xray.
 
  How you will get here:
  Education
 
   BS in Computer Science, Engineering or Mathematics and 2 – 5 years of related experience.
 
  Knowledge, Skills, Abilities
 
   Experience with software validation on embedded devices
   Ability to work with multi-disciplined, global teams
   Strong knowledge in understanding system functional requirements, test case development, test execution, defect reporting and verification.
   Experience within agile software development lifecycle processes
   Tools: Jira, Confluence and XRay
 
 
  Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory at Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
  Apply today! http://jobs.thermofisher.com
  Thermo Fisher Scientific is an EEO/Affirmative Action Employer and does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability or any other legally protected status.
  Accessibility/Disability Access
  Job Seekers with a Disability: Thermo Fisher Scientific offers accessibility service for job seekers requiring accommodations in the job application process. For example, this may include individuals requiring assistance because of hearing, vision, mobility, or cognitive impairments. If you are a job seeker with a disability, or assisting a person with a disability, and require accessibility assistance or an accommodation to apply for one of our jobs, please submit a request by telephone at 1-855-471-2255*. Please include your contact information and specific details about your required accommodation to support you during the job application process.
 
   This telephone line is reserved solely for job seekers with disabilities requiring accessibility assistance or an accommodation in the job application process. Messages left for other purposes, such as not being able to get into the career website, following up on an application, or other non-disability related technical issues will not receive a response.
 


Software Quality Assurance Engineer III - Thermo Fisher Scientific

Software Quality Assurance Engineer III

You should have significant experience in centralized monitoring, strong leadership skills, and a deep understanding of regulatory compliance and data analytics in a scientific context.

You will oversee centralized monitoring processes, ensure data integrity, lead teams, manage projects, and collaborate with cross-functional groups to optimize operational efficiency.

Dublin

<div>
 Work Schedule Standard (Mon-Fri)
 
 Environmental Conditions Office
 
 Job Description
 
 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
 
 The job:
 
 As Senior Director, Centralized Monitoring, you'll provide operational and strategic leadership for the development and delivery of Risk Based Quality Management (RBQM) strategy and centralized monitoring objectives. You will be responsible for directing, leading, and managing your assigned team to successfully complete CM deliverables in support of clients and studies. Your role will involve training, management, and mentorship within the department, as well as collaborative outreach to adjacent departments and functions.
 
 Our organisation:
 
 Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies.
 
 What will you do?
 
 
 <ul>
 <li> Serve as a Subject Matter Expert in Risk Based Quality Management (RBQM) methodologies, tools, processes, and central monitoring methods</li>
 <li> Develop and manage client and partner relationships, mentoring and directing staff and management, including overseeing and ensuring quality of RBQM and data strategy at the project and program level</li>
 <li> Drive risk assessment and define mitigations and proper monitoring strategy for critical data and processes</li>
 <li> Drive policy development and support implementation of broader goals by working across departments</li>
 <li> Supervise and coordinate centralized monitoring client risk and data strategy delivery</li>
 <li> Ensure the CM teams are provided with the necessary support and resources</li>
 <li> Manage staff and management, including interviewing, professional development, and performance management</li>
 <li> Lead internal and cross-functional initiatives, including process and tool development</li>
 <li> Contribute to future strategy and vision for CM and Clinical Operations</li>
 </ul>
 
 Who we are looking for:
 
 <ul>
 <li> Knowledge of broad drug development process and expertise in cross functional adoption of Risk Based Quality Management</li>
 <li> Knowledge of industry regulatory and clinical standards such as ICH E6 &amp; E8</li>
 <li> 15+ years of previous experience within Pharma or CRO organisations, providing the knowledge, skills, and abilities to perform the job</li>
 <li> Extensive prior management responsibility</li>
 <li> Advanced level of business English</li>
 </ul>
 
 What’s in it for you:
 
 We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!
</div>


 Work Schedule Standard (Mon-Fri)
 
  Environmental Conditions Office
 
  Job Description
 
  At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
 
  The job:
 
  As Senior Director, Centralized Monitoring, you'll provide operational and strategic leadership for the development and delivery of Risk Based Quality Management (RBQM) strategy and centralized monitoring objectives. You will be responsible for directing, leading, and managing your assigned team to successfully complete CM deliverables in support of clients and studies. Your role will involve training, management, and mentorship within the department, as well as collaborative outreach to adjacent departments and functions.
 
  Our organisation:
 
  Our global Clinical Operations colleagues within our PPD® clinical research services provide end-to-end support for clinical trials from study start up to monitoring through to study close out, across commercial and government contracts. Together, we help clients define and develop clinical programs, minimize delays, and implement high-quality, cost-efficient clinical studies.
 
  What will you do?
  
 
 
   Serve as a Subject Matter Expert in Risk Based Quality Management (RBQM) methodologies, tools, processes, and central monitoring methods
   Develop and manage client and partner relationships, mentoring and directing staff and management, including overseeing and ensuring quality of RBQM and data strategy at the project and program level
   Drive risk assessment and define mitigations and proper monitoring strategy for critical data and processes
   Drive policy development and support implementation of broader goals by working across departments
   Supervise and coordinate centralized monitoring client risk and data strategy delivery
   Ensure the CM teams are provided with the necessary support and resources
   Manage staff and management, including interviewing, professional development, and performance management
   Lead internal and cross-functional initiatives, including process and tool development
   Contribute to future strategy and vision for CM and Clinical Operations
 
 
  Who we are looking for:
 
 
   Knowledge of broad drug development process and expertise in cross functional adoption of Risk Based Quality Management
   Knowledge of industry regulatory and clinical standards such as ICH E6 & E8
   15+ years of previous experience within Pharma or CRO organisations, providing the knowledge, skills, and abilities to perform the job
   Extensive prior management responsibility
   Advanced level of business English
 
 
  What’s in it for you:
 
  We offer competitive remuneration, annual incentive plan bonus, healthcare, and a range of employee benefits. Thermo Fisher Scientific offers employment with an innovative, forward-thinking organization, and outstanding career and development prospects. We offer an exciting company culture that stands for integrity, intensity, involvement, and innovation!



Sr Director, Centralized Monitoring - Thermo Fisher Scientific

Sr Director, Centralized Monitoring

You need a relevant academic or vocational qualification in law and 0 to 2 years of experience to demonstrate the necessary knowledge and skills for this role.

You will draft, review, and negotiate complex agreements, address legal concerns, manage disputes, and improve processes while overseeing junior team members.

Legal

Job DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.We are currently hiring for an Associate Counsel Contracts to be based in Bulgaria, Italy or United Kingdom.<h2> A day in the Life:</h2><ul><li>Provides legal advice and support in the drafting, review and negotiation of agreements, working independently except for escalations where appropriate. Manages and negotiates language for more complex agreements (e.g. MSAs, quality agreements, and other unique non-standard contracts).</li><li>In addition to contracts, handles department matters and general legal concerns raised by internal customers and senior management, which may include without limitation initial dispute correspondence and other legal matters.</li><li>Leads the implementation of process improvement opportunities and oversees junior members of the department.</li></ul>Education:<ul><li>Relevant formal academic / vocational qualification in Low</li><li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).</li></ul>Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Job DescriptionAt Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.We are currently hiring for an Associate Counsel Contracts to be based in Bulgaria, Italy or United Kingdom. A day in the Life:Provides legal advice and support in the drafting, review and negotiation of agreements, working independently except for escalations where appropriate. Manages and negotiates language for more complex agreements (e.g. MSAs, quality agreements, and other unique non-standard contracts).In addition to contracts, handles department matters and general legal concerns raised by internal customers and senior management, which may include without limitation initial dispute correspondence and other legal matters.Leads the implementation of process improvement opportunities and oversees junior members of the department.Education:Relevant formal academic / vocational qualification in LowPrevious experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.

Associate Counsel Contracts - Thermo Fisher Scientific

United Kingdom

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 Job Description
 
 At Thermo Fisher Scientific, you’ll discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner and safer. We provide our teams with the resources needed to achieve individual career goals while taking science a step beyond through research, development and delivery of life-changing therapies. With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities depend on – now and in the future.
 
 We are currently hiring for an Associate Counsel Contracts to be based in Bulgaria, Italy or United Kingdom.
 <h2 class="jobSectionHeader"> A day in the Life:</h2>
 <ul>
 <li> Provides legal advice and support in the drafting, review and negotiation of agreements, working independently except for escalations where appropriate. Manages and negotiates language for more complex agreements (e.g. MSAs, quality agreements, and other unique non-standard contracts).</li>
 <li> In addition to contracts, handles department matters and general legal concerns raised by internal customers and senior management, which may include without limitation initial dispute correspondence and other legal matters.</li>
 <li> Leads the implementation of process improvement opportunities and oversees junior members of the department.</li>
 </ul>
 
 <h2 class="jobSectionHeader"> Education:</h2>
 <ul>
 <li> Relevant formal academic / vocational qualification in Low </li>
 <li>Previous experience that provides the knowledge, skills, and abilities to perform the job (comparable to 0 to 2 years).</li>
 </ul>
 
 <div>
 Our Mission is to enable our customers to make the world healthier, cleaner and safer. Watch as our colleagues explain 5 reasons to work with us. As one team of 100,000+ colleagues, we share a common set of values - Integrity, Intensity, Innovation and Involvement - working together to accelerate research, solve complex scientific challenges, drive technological innovation and support patients in need. #StartYourStory with PPD, part of Thermo Fisher Scientific, where diverse experiences, backgrounds and perspectives are valued.
 
 <h2 class="jobSectionHeader"> Apply today! http://jobs.thermofisher.com</h2>
 </div>
</div>

Thermo Fisher Scientific

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