Biogen
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We work toward one goal: to improve the lives of people coping with serious disease. Getting there requires the coordinated efforts of many business areas, each with its own focus.

 

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D+I at Biogen

Workforce Diversity

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At Biogen, we believe diversity fuels excellence. Our organization has nearly 7,000 employees in over 30 countries, so we rely on these different perspectives to achieve business success, contribute to a healthier society, and bring unprecedented, innovative solutions to the patients and communities we serve.

Biogen Jobs

Engineer I/II, Validation
SummaryThe incumbent coordinates and supports validation related to manufacturing and environmentally controlled equipment; provides on-the-floor-support, tracking and updates by performing duties personally or through subordinate supervisors. In addition, this role also supports project initiatives related to general validation projects, validation compliance deliverables and reports, and validation system improvements and/or execution.Job DescriptionThe Validation Engineer I/II is responsible for supporting Cleanability Testing and for providing a variety of GMP processes to validate the cleanability of surface area samples. These services include preparation of complex proteins, documenting how they react with certain cleaning products, operating cleaning equipment, and performing TOC prep/analysis. The cleanability study will compare seven different product contact surfaces (i.e. acrylic, glass, EPDM, viton, silicone, Teflon, and stainless steel) which are used in the Biogen manufacturing facilities. Additional responsibilities include but are not limited to:*Authors sections of Validation-related reports \u0026 project plans, provides technical evaluations of validation requirements for global change controls and associated action plans*Specifically designs \u0026 develops validation protocols, provides expertise to associated equipment \u0026 automation design / modifications*Coordinates equipment validation protocols (development \u0026 management) for specific equipment areas - including presentation of technical training \u0026 support to personnel, with on-floor guidance.Qualifications*Two to five (2-5) years related experience. *Industry Knowledge on GMPs and FDA audits*Experience in Cleaning and Equipment Validation Philosophy*Practical knowledge and application of GMP and EMEA regulations*Experience in pharmaceutical or biotech manufacturing environmentEducationBachelor's degree requiredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
Engineer I/II, Validation
SummaryThe incumbent coordinates and supports validation related to manufacturing and environmentally controlled equipment; provides on-the-floor-support, tracking and updates by performing duties personally or through subordinate supervisors. In addition, this role also supports project initiatives related to general validation projects, validation compliance deliverables and reports, and validation system improvements and/or execution.Job DescriptionThe Validation Engineer I/II is responsible for supporting Cleanability Testing and for providing a variety of GMP processes to validate the cleanability of surface area samples. These services include preparation of complex proteins, documenting how they react with certain cleaning products, operating cleaning equipment, and performing TOC prep/analysis. The cleanability study will compare seven different product contact surfaces (i.e. acrylic, glass, EPDM, viton, silicone, Teflon, and stainless steel) which are used in the Biogen manufacturing facilities. Additional responsibilities include but are not limited to:*Authors sections of Validation-related reports \u0026 project plans, provides technical evaluations of validation requirements for global change controls and associated action plans*Specifically designs \u0026 develops validation protocols, provides expertise to associated equipment \u0026 automation design / modifications*Coordinates equipment validation protocols (development \u0026 management) for specific equipment areas - including presentation of technical training \u0026 support to personnel, with on-floor guidance.Qualifications*Two to five (2-5) years related experience. *Industry Knowledge on GMPs and FDA audits*Experience in Cleaning and Equipment Validation Philosophy*Practical knowledge and application of GMP and EMEA regulations*Experience in pharmaceutical or biotech manufacturing environmentEducationBachelor's degree requiredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
Sr. Program Manager -Digital Services
SummaryAs the Sr. Program Manager, you will be responsible for leading and managing all aspects Patient Services' digital delivery transformation and integration within Patient Services technology platforms. This role will be a digital counterpart collaborating with our Multi-Channel Excellence team to drive optimization and enhancement to our customer experience through extending our digital services capabilities.Job DescriptionAs the Sr. Program Manager, you will be responsible for leading and managing all aspects Patient Services' digital delivery transformation and integration within Patient Services technology platforms. This role will be a digital counterpart collaborating with our Multi-Channel Excellence team to drive optimization and enhancement to our customer experience through extending our digital services capabilities. Digital services include portals, mobile apps, text and chat communication channels and other technology solutions to address customer needs. Thus, the ideal candidate will have a strong Patient Services process background with examples of successfully leading diverse, cross-functional teams in the development and execution of complex tactical initiatives. What should shine through is his/her ability to draw on customer and competitive insights, pro-actively communicate and collaborate, and execute with a strong sense of urgency. The candidate would also preferably have customer-facing experience, as well as the ability to assimilate key insights and the consequences of such findings into the development of services and solutions that exceed customer expectations. Essential functions of the job include: * Demonstrate strong leadership of large, disruptive and complex initiatives that support Biogen's "Trust and Value" remit * Develop a deep understanding of the customer's mindset to ensure services and solutions create an optimal customer experience through build of MyBiogen portal* Influence, collaborate and pro-actively communicate with cross-functional stakeholders at all levels of the organization, as well as key external business partners, to ensure team alignment* Help lay the groundwork for a patient services and solutions strategic roadmap and branding* Monitor the competitive landscape to ensure we evolve MyBiogen Portal's development to maintain best-in-class services and solutionsQualificationsThe ideal candidate will have a track record of: * Strong strategic thinking: Demonstrate an ability to independently identify and develop the ideal approach to solve moderately to highly complex marketing or cross-functional projects with limited guidance* Effective communication skills and executive presence: Be pro-active in verbal and written communications at all levels of the organization * Strong cross-functional collaboration: Collaborate effectively with various functional partners by asking questions, gathering required information for analysis and influencing across the organization to drive results* Disciplined project management: Deliver clear, integrated, multi-audience plans that support a portfolio approach and can be effectively implemented* Strong personal drive: Take an action-oriented approach with a demonstrated ability to synthesize customer needs with business needs, independently prioritize, problem solve and execute the plan in a fast-paced and ambiguous environmentRequirements: * At least 7-10 years of experience in project management * Patient Services experience preferred * System/portal launch experience preferred * Entrepreneurial spirit /Exceptional work ethic, sense of urgency, and execution-orientation* Predisposition to ask the extra questions needed to fully understand and create the best work product* Deep customer understanding and focus * High comfort with articulating vision orally and through powerpoint* Demonstrated analysis and problem-solving skills required* Positive team player * Strong written and verbal communication * Ability to drive change management processes* Highly self-motivated, confident, high-energy and bright individual with an ability to operate independently without strong support or guidance* Travel 10%EducationBachelor's Degree RequiredMaster's Degree PreferredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
Sr. Program Manager -Digital Services
SummaryAs the Sr. Program Manager, you will be responsible for leading and managing all aspects Patient Services' digital delivery transformation and integration within Patient Services technology platforms. This role will be a digital counterpart collaborating with our Multi-Channel Excellence team to drive optimization and enhancement to our customer experience through extending our digital services capabilities.Job DescriptionAs the Sr. Program Manager, you will be responsible for leading and managing all aspects Patient Services' digital delivery transformation and integration within Patient Services technology platforms. This role will be a digital counterpart collaborating with our Multi-Channel Excellence team to drive optimization and enhancement to our customer experience through extending our digital services capabilities. Digital services include portals, mobile apps, text and chat communication channels and other technology solutions to address customer needs. Thus, the ideal candidate will have a strong Patient Services process background with examples of successfully leading diverse, cross-functional teams in the development and execution of complex tactical initiatives. What should shine through is his/her ability to draw on customer and competitive insights, pro-actively communicate and collaborate, and execute with a strong sense of urgency. The candidate would also preferably have customer-facing experience, as well as the ability to assimilate key insights and the consequences of such findings into the development of services and solutions that exceed customer expectations. Essential functions of the job include: * Demonstrate strong leadership of large, disruptive and complex initiatives that support Biogen's "Trust and Value" remit * Develop a deep understanding of the customer's mindset to ensure services and solutions create an optimal customer experience through build of MyBiogen portal* Influence, collaborate and pro-actively communicate with cross-functional stakeholders at all levels of the organization, as well as key external business partners, to ensure team alignment* Help lay the groundwork for a patient services and solutions strategic roadmap and branding* Monitor the competitive landscape to ensure we evolve MyBiogen Portal's development to maintain best-in-class services and solutionsQualificationsThe ideal candidate will have a track record of: * Strong strategic thinking: Demonstrate an ability to independently identify and develop the ideal approach to solve moderately to highly complex marketing or cross-functional projects with limited guidance* Effective communication skills and executive presence: Be pro-active in verbal and written communications at all levels of the organization * Strong cross-functional collaboration: Collaborate effectively with various functional partners by asking questions, gathering required information for analysis and influencing across the organization to drive results* Disciplined project management: Deliver clear, integrated, multi-audience plans that support a portfolio approach and can be effectively implemented* Strong personal drive: Take an action-oriented approach with a demonstrated ability to synthesize customer needs with business needs, independently prioritize, problem solve and execute the plan in a fast-paced and ambiguous environmentRequirements: * At least 7-10 years of experience in project management * Patient Services experience preferred * System/portal launch experience preferred * Entrepreneurial spirit /Exceptional work ethic, sense of urgency, and execution-orientation* Predisposition to ask the extra questions needed to fully understand and create the best work product* Deep customer understanding and focus * High comfort with articulating vision orally and through powerpoint* Demonstrated analysis and problem-solving skills required* Positive team player * Strong written and verbal communication * Ability to drive change management processes* Highly self-motivated, confident, high-energy and bright individual with an ability to operate independently without strong support or guidance* Travel 10%EducationBachelor's Degree RequiredMaster's Degree PreferredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
Engineer II/III, Validation
SummaryThe incumbent leads or co-leads project initiatives related to global alignment of automation validation practices, site validation innovation, improvements, and/or execution. This role will develops software test protocols in support of change controls, new products and processes.Job DescriptionThe Validation Engineer II/III represents or co-represents the validation department/function/company during internal/external audits and regulatory inspections. Additional responsibilities include but are not limited to:*Provides guidance / leadership to junior associates where applicable. *Leads or co-leads coordination and support of all automation validation related to Biogen's manufacturing equipment, utilities, and facilities*Provides on the floor execution support, tracking, and updates by performing duties personally or through subordinate contractors or dotted line reports. *Provides input \u0026 validation guidance to Tech Transfer and project / area efforts, provides technical evaluations of validation requirements for automation change controls \u0026 associated action plans.Qualifications*Minimum of five (5) years related experience in DeltaV or other DCS System; or Master's degree with minimum of three (3) years related experience. *Basic knowledge on GMPs and FDA audits*Experience in Automation Validation Philosophy. *Knowledge of GMP and EMEA regulations. *Experience in pharmaceutical or biotech manufacturing environment and in coordinating / co-leading cross-site or cross-functional initiatives.EducationBachelor's degree in engineering requiredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
Engineer II/III, Validation
SummaryThe incumbent leads or co-leads project initiatives related to global alignment of automation validation practices, site validation innovation, improvements, and/or execution. This role will develops software test protocols in support of change controls, new products and processes.Job DescriptionThe Validation Engineer II/III represents or co-represents the validation department/function/company during internal/external audits and regulatory inspections. Additional responsibilities include but are not limited to:*Provides guidance / leadership to junior associates where applicable. *Leads or co-leads coordination and support of all automation validation related to Biogen's manufacturing equipment, utilities, and facilities*Provides on the floor execution support, tracking, and updates by performing duties personally or through subordinate contractors or dotted line reports. *Provides input \u0026 validation guidance to Tech Transfer and project / area efforts, provides technical evaluations of validation requirements for automation change controls \u0026 associated action plans.Qualifications*Minimum of five (5) years related experience in DeltaV or other DCS System; or Master's degree with minimum of three (3) years related experience. *Basic knowledge on GMPs and FDA audits*Experience in Automation Validation Philosophy. *Knowledge of GMP and EMEA regulations. *Experience in pharmaceutical or biotech manufacturing environment and in coordinating / co-leading cross-site or cross-functional initiatives.EducationBachelor's degree in engineering requiredAll individuals deserve the right to achieve their full potential. Accordingly, our company welcomes all job applicants, and we strive to provide all employees with equal opportunity for advancement. We will not tolerate any form of discrimination or harassment based on an individual's 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 local government agencies or law.As an employer of choice, we strive to:Provide attractive employment opportunities for diverse candidates at all levels and in all segments of our organizationPursue and maintain relationships with sources of diverse candidates, community organizations, and academic institutionsComply with both the letter and the spirit of all applicable laws and regulations relating to nondiscrimination and affirmative action in employmentVEVRAA Federal ContractorWe Request Priority Protected Veteran and Disabled Referrals for all of our locations
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