Medical, vision and dental plans

On-site fitness centers, with allowances or reimbursement options

Competitive compensation

Retirement or savings plans

Generous paid time off

Flexible work arrangements and summer hours

Sick Pay

Large

Customer Focused

Inclusive

Pioneering

Agile

Accountable

Ethical

Biogen is a global biotechnology company that specialises in the discovery, development, and delivery of innovative therapies for neurological and neurodegenerative diseases. They focus on researching and creating treatments for conditions such as multiple sclerosis (MS), spinal muscular atrophy (SMA), and Alzheimer's disease. Biogen's ultimate mission is to pioneer new approaches in biotechnology to address unmet medical needs and improve the lives of patients worldwide. Their purpose is to transform scientific discoveries into therapies that have a significant impact on patients' lives, aiming to provide hope, relief, and improved outcomes for individuals suffering from debilitating neurological disorders. Biogen's commitment lies in advancing the understanding and treatment of neurological conditions through cutting-edge research, development of innovative therapies, and collaboration with healthcare professionals and patient communities.

Science & Healthcare

Biogen

Biopharmaceutical

You must be a final year Master's student in Business, Life Sciences, or Analytics, with Excel mastery, fluent English, and strong analytical, communication, and organizational skills.

You will support forecasts, integrate insights, streamline processes, aid Brand Leads, automate reports, coordinate market research, and enhance market understanding through competitive intelligence.

Data

Business, Operations & Strategy

Madrid

<div>
 Job Description
 Biogen y el programa BioRace:
 Biogen es una de las empresas biotecnológicas líderes en el mundo que está especialmente dedicada al desarrollo de terapias para trastornos neurodegenerativos, autoinmunes y enfermedades raras.
 Con el objetivo de atraer y formar al mejor talento, Biogen ha creado un nuevo programa anual de becas: BioRace.
 BioRace proporciona a los estudiantes la oportunidad de poner en práctica sus conocimientos académicos en un contexto empresarial muy dinámico y retador, que les ayudará a crecer y que les servirá de palanca para su desarrollo profesional.
 BioRace se basa en 5 pilares para la formación y desarrollo de sus participantes:
 <ul>
 <li>Formaciones científicas, técnicas y en soft skills.</li>
 <li>Salidas al campo con Medical Science Liaisons, Key Account Managers y/o equipos de ventas.</li>
 <li>Seguimiento continuo con Recursos Humanos y sus tutores.</li>
 <li>Cafés virtuales bimensuales con los miembros del Comité de Dirección de Biogen y con personas trabajadoras referentes de la compañía.</li>
 <li>Dos proyectos que pondrán a prueba todas las habilidades y conocimientos adquiridos durante la formación en Biogen.</li>
 </ul>
 Position Summary:
 The CMI Trainee will be a member of the CE&amp;O department, working closely with CMI Sr Manager in generating strategic insights on Iberia cluster, on performance and market dynamics monitoring, utilizing primary and secondary market research, as well as internal and external quantitative data sources and advanced analytics.
 Responsibilities:
 Forecasting &amp; Analytics:
 <ul>
 <li>Supporting the development of our monthly forecasts, providing input into scenarios, assumptions, and key market events</li>
 <li>Applying analytical expertise to support insight generation process, integrating various qualitative and quantitative sources</li>
 <li>Leveraging analytical expertise to align and support organization during business reviews, annual operating planning and management meeting</li>
 <li>Supporting the CMI team in streamlining processes and automating analytical tools and models</li>
 </ul>
 Business Performance Assessment:
 <ul>
 <li>Supporting Brand Leads providing a thorough understanding of the market and brand performance</li>
 <li>Contributing to developing and automating performance reports, used to tracks performance vs target and KPIs</li>
 </ul>
 Market research &amp; Competitor Intelligence 
 <ul>
 <li>Coordinating assigned MR within CMI team and identifying gaps and needs to help elevate the level of understanding within the team and among key stakeholders</li>
 <li>Identifying and collating CI helping add further depth to our market understanding</li>
 </ul> Qualifications 
 <ul>
 <li>Final year of Master's degree in Business Administration, Life Sciences or Business Analytics</li>
 <li>Excellent mastery of Excel</li>
 <li>Fluent in English, written and spoken</li>
 <li>Knowledge Power BI tool will be desirable</li>
 <li>Analytical, pragmatic, and logical mindset</li>
 <li>Innovative mindset</li>
 <li>Ability to create clear summaries and defend strong recommendations</li>
 <li>Client-oriented – responsiveness, flexibility, adaptability</li>
 <li>Interpersonal skills (listening and communication)</li>
 <li>Autonomy and organizational skills</li>
 </ul> Additional Information
 Datos importantes:
 <ul>
 <li>Área funcional: departamento Customer &amp; Market Insights</li>
 <li>Duración de la beca: 12 meses.</li>
 <li>Fecha de incorporación: 14 de octubre 2024.</li>
 <li>Horario: de 9:00 a 17:30 de lunes a jueves (con una hora para comer) y de 8:00 a 15:00 los viernes.</li>
 <li>Dirección: Paseo de la Castellana, nº41. 28046 Madrid.</li>
 <li>Ayuda a la beca: 800€ brutos/mes.</li>
 <li>Tique restaurante: 200€/mes (excepto durante el mes de agosto).</li>
 </ul>
 <div></div>
 Why Biogen?
 We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
 At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&amp;I efforts.
</div>


 Job Description
  Biogen y el programa BioRace:
 Biogen es una de las empresas biotecnológicas líderes en el mundo que está especialmente dedicada al desarrollo de terapias para trastornos neurodegenerativos, autoinmunes y enfermedades raras.
 Con el objetivo de atraer y formar al mejor talento, Biogen ha creado un nuevo programa anual de becas: BioRace.
 BioRace proporciona a los estudiantes la oportunidad de poner en práctica sus conocimientos académicos en un contexto empresarial muy dinámico y retador, que les ayudará a crecer y que les servirá de palanca para su desarrollo profesional.
 BioRace se basa en 5 pilares para la formación y desarrollo de sus participantes:
 
  Formaciones científicas, técnicas y en soft skills.
  Salidas al campo con Medical Science Liaisons, Key Account Managers y/o equipos de ventas.
  Seguimiento continuo con Recursos Humanos y sus tutores.
  Cafés virtuales bimensuales con los miembros del Comité de Dirección de Biogen y con personas trabajadoras referentes de la compañía.
  Dos proyectos que pondrán a prueba todas las habilidades y conocimientos adquiridos durante la formación en Biogen.
 
  Position Summary:
 The CMI Trainee will be a member of the CE&O department, working closely with CMI Sr Manager in generating strategic insights on Iberia cluster, on performance and market dynamics monitoring, utilizing primary and secondary market research, as well as internal and external quantitative data sources and advanced analytics.
  Responsibilities:
  Forecasting & Analytics:
 
  Supporting the development of our monthly forecasts, providing input into scenarios, assumptions, and key market events
  Applying analytical expertise to support insight generation process, integrating various qualitative and quantitative sources
  Leveraging analytical expertise to align and support organization during business reviews, annual operating planning and management meeting
  Supporting the CMI team in streamlining processes and automating analytical tools and models
 
  Business Performance Assessment:
 
  Supporting Brand Leads providing a thorough understanding of the market and brand performance
  Contributing to developing and automating performance reports, used to tracks performance vs target and KPIs
 
  Market research & Competitor Intelligence 
 
  Coordinating assigned MR within CMI team and identifying gaps and needs to help elevate the level of understanding within the team and among key stakeholders
  Identifying and collating CI helping add further depth to our market understanding
   Qualifications
 
  Final year of Master's degree in Business Administration, Life Sciences or Business Analytics
  Excellent mastery of Excel
  Fluent in English, written and spoken
  Knowledge Power BI tool will be desirable
  Analytical, pragmatic, and logical mindset
  Innovative mindset
  Ability to create clear summaries and defend strong recommendations
  Client-oriented – responsiveness, flexibility, adaptability
  Interpersonal skills (listening and communication)
  Autonomy and organizational skills
   Additional Information
  Datos importantes:
 
  Área funcional: departamento Customer & Market Insights
  Duración de la beca: 12 meses.
  Fecha de incorporación: 14 de octubre 2024.
  Horario: de 9:00 a 17:30 de lunes a jueves (con una hora para comer) y de 8:00 a 15:00 los viernes.
  Dirección: Paseo de la Castellana, nº41. 28046 Madrid.
  Ayuda a la beca: 800€ brutos/mes.
  Tique restaurante: 200€/mes (excepto durante el mes de agosto).
 
 
  Why Biogen?
 We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
 At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.


Intern, Customer & Market Insights (12 meses - Convenio imprescindible) - Biogen

Intern, Customer & Market Insights (12 meses - Convenio imprescindible)

You must have a Law degree, 6+ years as an attorney, strong contract knowledge, compliance focus, and fluency in English and Spanish. Pharmaceutical experience is a plus.

You will manage contracts, coordinate with teams, provide training, support legal and compliance functions, handle vendor communication, and oversee data privacy in Iberia.

<div>
 Job Description
 The role of the Contract Manager is an operational role whose primary function is being an advisor and business partner to the Iberia Cluster to better contract with external stakeholders, providing guidance to all functions on contract related matters.
 It requires:
 <ul>
 <li>A strong legal contract knowledge.</li>
 <li>A compliance driven mentality.</li>
 </ul>
 A proactive hands-on approach, capacity to work with autonomy, and “business partner” mentality.
 CONTRACT MANAGEMENT
 <ul>
 <li>Serve as primary contract manager of the Iberia Cluster (Spain and Portugal). Prepare, and review agreements (e.g. clinical trial, healthcare related agreements, commercial agreements, vendor and supplier agreements, CDA, etc.).</li>
 <li>Coordination with assistants and other Biogen affiliate and international teams in the contract management process.</li>
 <li>Cooperation in the contract/addendum/master template creation and implementation.</li>
 <li>Liaison with Legal Corporate function for the contract local needs analysis, contract template creation, modification and approval, master agreements included.</li>
 <li>Owner for contracts and addendums database, keeping them up to date.</li>
 <li>Communication with vendors and/or service providers as necessary to resolve contract issues.</li>
 <li>Acts as a first point of contact for inquiries on contracts for commercial functions within the affiliate and provide guidance on contract and addendum.</li>
 <li>Monitoring and follows up on framework agreements signed and their renewal/extension/close-out.</li>
 <li>Creation and delivers trainings to managers and all employees on contract management.</li>
 <li>Supports Corporate Administration activities including but not limited to:</li>
 </ul>
 Provides support on corporate administration activities (BoD, Shareholders meeting, Power of Attorney etc.) coordinating with legal Corporate function where appropriate.
 <ul>
 <li>Clinical Trials: supports and provides guidance, within the Clinical Trials framework, on contractual and legal related activities/matters acting as a first point of contact for internal stakeholders.</li>
 </ul>
 LEGAL
 Closely collaborate and support the Legal function on Iberia Cluster legal matters, contracts, and general corporate and pharmaceutical law in relation to commercialization of biopharmaceutical products, including sales, marketing, and distribution, as well as medical affairs activities.
 COMPLIANCE
 Closely collaborate and support the Compliance function on Iberia Cluster on compliance and governance risk pertaining to the commercialization of biopharmaceutical products, including sales, marketing, and distribution, as well as medical affairs activities.
 FINANCE
 Closely collaborate and support the Finance function in relation to procurement processes, vendors, and others related to the Iberia cluster activities (including primary owner for VRM)
 DATA PRIVACY
 Lead Data privacy activities in the Iberia Cluster Qualifications 
 <ul>
 <li>Degree in Law.</li>
 <li>Fluent in English and Spanish; preferred fluent in Portuguese.</li>
 <li>6+ years of experience as an attorney (law firm or in house).</li>
 <li>Strong experience in Contracts.</li>
 <li>International experience a plus.</li>
 <li>Experience/knowledge in Pharmaceutical, Healthcare, Life Science sector and/or regulated environments / compliance related to FCPA.</li>
 <li>Organizational skills and management of different teams.</li>
 <li>Results oriented, with a high level of autonomy.</li>
 </ul> Additional Information
 <div></div>
 Why Biogen?
 We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
 At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&amp;I efforts.
</div>


 Job Description
  The role of the Contract Manager is an operational role whose primary function is being an advisor and business partner to the Iberia Cluster to better contract with external stakeholders, providing guidance to all functions on contract related matters.
 It requires:
 
  A strong legal contract knowledge.
  A compliance driven mentality.
 
 A proactive hands-on approach, capacity to work with autonomy, and “business partner” mentality.
  CONTRACT MANAGEMENT
 
  Serve as primary contract manager of the Iberia Cluster (Spain and Portugal). Prepare, and review agreements (e.g. clinical trial, healthcare related agreements, commercial agreements, vendor and supplier agreements, CDA, etc.).
  Coordination with assistants and other Biogen affiliate and international teams in the contract management process.
  Cooperation in the contract/addendum/master template creation and implementation.
  Liaison with Legal Corporate function for the contract local needs analysis, contract template creation, modification and approval, master agreements included.
  Owner for contracts and addendums database, keeping them up to date.
  Communication with vendors and/or service providers as necessary to resolve contract issues.
  Acts as a first point of contact for inquiries on contracts for commercial functions within the affiliate and provide guidance on contract and addendum.
  Monitoring and follows up on framework agreements signed and their renewal/extension/close-out.
  Creation and delivers trainings to managers and all employees on contract management.
  Supports Corporate Administration activities including but not limited to:
 
 Provides support on corporate administration activities (BoD, Shareholders meeting, Power of Attorney etc.) coordinating with legal Corporate function where appropriate.
 
  Clinical Trials: supports and provides guidance, within the Clinical Trials framework, on contractual and legal related activities/matters acting as a first point of contact for internal stakeholders.
 
  LEGAL
 Closely collaborate and support the Legal function on Iberia Cluster legal matters, contracts, and general corporate and pharmaceutical law in relation to commercialization of biopharmaceutical products, including sales, marketing, and distribution, as well as medical affairs activities.
  COMPLIANCE
 Closely collaborate and support the Compliance function on Iberia Cluster on compliance and governance risk pertaining to the commercialization of biopharmaceutical products, including sales, marketing, and distribution, as well as medical affairs activities.
  FINANCE
 Closely collaborate and support the Finance function in relation to procurement processes, vendors, and others related to the Iberia cluster activities (including primary owner for VRM)
  DATA PRIVACY
 Lead Data privacy activities in the Iberia Cluster Qualifications
 
  Degree in Law.
  Fluent in English and Spanish; preferred fluent in Portuguese.
  6+ years of experience as an attorney (law firm or in house).
  Strong experience in Contracts.
  International experience a plus.
  Experience/knowledge in Pharmaceutical, Healthcare, Life Science sector and/or regulated environments / compliance related to FCPA.
  Organizational skills and management of different teams.
  Results oriented, with a high level of autonomy.
   Additional Information
 
  Why Biogen?
 We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
 At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.


Manager, Contract Operations - Iberia - Biogen

Manager, Contract Operations - Iberia

You need a Bachelor's in Engineering, 10+ years in Combination Product R&D or Device Quality, strong in design controls, risk management, and regulatory filings. Skills in project management and communication are essential.

You will guide quality engineering in combination products, lead Design Control, ensure compliance, manage supplier relations, drive QMS improvements, support regulatory filings, and participate in audits.

Cambridge

<div>
 Job Description
 Biogen is seeking a seasoned Senior Principal Combination Product Quality Engineer to serve as an Associate Director within our Quality, Combination Products, and Devices team. In this role, you will provide comprehensive quality oversight for the lifecycle management of combination products. Your expertise in design control, risk management, and human factor engineering will drive continuous improvement efforts and ensure compliance with local and global regulations. You will play a critical role in shaping our design and development processes, contributing to regulatory strategies, and managing external partnerships.
 What You’ll Do:
 <ul>
 <li> Provide Subject Matter Expertise in combination products, guiding quality engineering function on related issues.</li>
 </ul>
 <ul>
 <li> Lead the execution of Design Control processes across all stages of product development.</li>
 </ul>
 <ul>
 <li> Ensure compliance with global quality standards by reviewing and approving technical documentation.</li>
 </ul>
 <ul>
 <li> Guide R&amp;D and manufacturing design processes to implement effective Design Control principles.</li>
 </ul>
 <ul>
 <li> Manage external relationships with device suppliers and testing partners, ensuring adherence to quality standards.</li>
 </ul>
 <ul>
 <li> Spearhead continuous improvement initiatives within the device and combination product Quality Management System (QMS).</li>
 </ul>
 <ul>
 <li> Support regulatory filings and audits, acting as the final Quality approval authority for device sections.</li>
 </ul>
 <ul>
 <li> Participate in internal and external audits and facilitate regulatory inspections.</li>
 </ul>
 Who You Are: You are a forward-thinking R&amp;D engineer with a keen interest in end-to-end quality engineering and risk management with recognized expertise in executing within medical device, biopharmaceutical and combination products sectors. Your innovative approach and statistical acumen make you natural at navigating the complexities of device quality in the biotechnology field. You possess a passion to optimize Quality Management Systems (QMS) from a compliance function to a proactive business enabler tool to address patients’ unmet needs. You are a recognized SME with execution record in end-to-end Design Control, Risk Management, Post Market Surveillance, and Human Factor Engineering for complex combination products. #LI-CC1 Qualifications
 Required Skills:
 <ul>
 <li> Bachelor's Degree in Engineering</li>
 </ul>
 <ul>
 <li> Minimum 10 years' experience in Combination Product R&amp;D or Device Quality Engineering within the Pharmaceutical/Biotech industries.</li>
 </ul>
 <ul>
 <li> Proficient understanding of Design Controls, cGMP, ISO 13485, QSR (21 CFR Part 820), and ISO 14971.</li>
 </ul>
 <ul>
 <li> Proven track record in verification &amp; validation plans and user needs translation.</li>
 </ul>
 <ul>
 <li> Strong grasp of Risk Management for combination products and medical devices.</li>
 </ul>
 <ul>
 <li> Familiar with statistical tools and validation/verification techniques.</li>
 </ul>
 <ul>
 <li> Demonstrated ability in regulatory filings and inspection facilitation.</li>
 </ul>
 <ul>
 <li> Experience in matrix organization and exceptional communication skills.</li>
 </ul>
 <ul>
 <li> Strong project management, negotiation, and interpersonal skills.</li>
 </ul>
 Preferred Skills:
 <ul>
 <li> Master’s degree with 8+ years or a PhD with 4+ years of experience in Combination Product R&amp;D or Device Quality Engineering within the Pharmaceutical/Biotech industries</li>
 </ul>
 <ul>
 <li> Experience with Class III medical devices.</li>
 </ul>
 <ul>
 <li> Quality certifications (e.g., CQE, Six Sigma).</li>
 </ul>
 <ul>
 <li> 1+ years of people management experience.</li>
 </ul> Additional Information
 <div></div>
 Why Biogen?
 We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
 At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&amp;I efforts.
 All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.
</div>


 Job Description
  Biogen is seeking a seasoned Senior Principal Combination Product Quality Engineer to serve as an Associate Director within our Quality, Combination Products, and Devices team. In this role, you will provide comprehensive quality oversight for the lifecycle management of combination products. Your expertise in design control, risk management, and human factor engineering will drive continuous improvement efforts and ensure compliance with local and global regulations. You will play a critical role in shaping our design and development processes, contributing to regulatory strategies, and managing external partnerships.
  What You’ll Do:
 
   Provide Subject Matter Expertise in combination products, guiding quality engineering function on related issues.
 
 
   Lead the execution of Design Control processes across all stages of product development.
 
 
   Ensure compliance with global quality standards by reviewing and approving technical documentation.
 
 
   Guide R&D and manufacturing design processes to implement effective Design Control principles.
 
 
   Manage external relationships with device suppliers and testing partners, ensuring adherence to quality standards.
 
 
   Spearhead continuous improvement initiatives within the device and combination product Quality Management System (QMS).
 
 
   Support regulatory filings and audits, acting as the final Quality approval authority for device sections.
 
 
   Participate in internal and external audits and facilitate regulatory inspections.
 
  Who You Are: You are a forward-thinking R&D engineer with a keen interest in end-to-end quality engineering and risk management with recognized expertise in executing within medical device, biopharmaceutical and combination products sectors. Your innovative approach and statistical acumen make you natural at navigating the complexities of device quality in the biotechnology field. You possess a passion to optimize Quality Management Systems (QMS) from a compliance function to a proactive business enabler tool to address patients’ unmet needs. You are a recognized SME with execution record in end-to-end Design Control, Risk Management, Post Market Surveillance, and Human Factor Engineering for complex combination products. #LI-CC1 Qualifications
  Required Skills:
 
   Bachelor's Degree in Engineering
 
 
   Minimum 10 years' experience in Combination Product R&D or Device Quality Engineering within the Pharmaceutical/Biotech industries.
 
 
   Proficient understanding of Design Controls, cGMP, ISO 13485, QSR (21 CFR Part 820), and ISO 14971.
 
 
   Proven track record in verification & validation plans and user needs translation.
 
 
   Strong grasp of Risk Management for combination products and medical devices.
 
 
   Familiar with statistical tools and validation/verification techniques.
 
 
   Demonstrated ability in regulatory filings and inspection facilitation.
 
 
   Experience in matrix organization and exceptional communication skills.
 
 
   Strong project management, negotiation, and interpersonal skills.
 
  Preferred Skills:
 
   Master’s degree with 8+ years or a PhD with 4+ years of experience in Combination Product R&D or Device Quality Engineering within the Pharmaceutical/Biotech industries
 
 
   Experience with Class III medical devices.
 
 
   Quality certifications (e.g., CQE, Six Sigma).
 
 
   1+ years of people management experience.
  Additional Information
 
  Why Biogen?
  We are a global team with a commitment to excellence, and a pioneering spirit. As a mid-sized biotechnology company, we provide the stability and resources of a well-established business while fostering an environment where individual contributions make a significant impact. Our team encompasses some of the most talented and passionate achievers who have unparalleled opportunities for learning, growth, and expanding their skills. Above all, we work together to deliver life-changing medicines, with every role playing a vital part in our mission. Caring Deeply. Achieving Excellence. Changing Lives.
  At Biogen, we are committed to building on our culture of inclusion and belonging that reflects the communities where we operate and the patients we serve. We know that diverse backgrounds, cultures, and perspectives make us a stronger and more innovative company, and we are focused on building teams where every employee feels empowered and inspired. Read on to learn more about our DE&I efforts.
  All qualified applicants will receive consideration for employment without regard to sex, gender identity or expression, sexual orientation, marital status, race, color, national origin, ancestry, ethnicity, religion, age, veteran status, disability, genetic information or any other basis protected by federal, state or local law. Biogen is an E-Verify Employer in the United States.

