Biogen
At Biogen, we develop, market and manufacture therapies for people living with serious neurological, autoimmune and hematologic disorders.
Header_biogen-talent_comm-header-670x140

Tweets by Biogen

Join Us

1426872628716

Explore career opportunities at Biogen, and experience the fulfillment that comes from helping to discover, manufacture and market new treatments for patients.

Biogen, On Again

Workforce Diversity

1426872567490

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

Scientist I / II, Drug Product Delivery, Antisense Oligonucleotide (AS
SummaryAs a member of Biogen's Antisense Oligonucleotide Drug Product development team, the candidate will dive a cross-functional team evaluating antisense oligonucleotide (ASO) drug delivery platforms.Job DescriptionThe candidate will be responsible for formulation and process development activities of ASO drug product development programs. Conducting in-house laboratory studies and managing technical work with manufacturing facilities is a requirement of the position. Candidate is expected to work collaboratively in a matrix environment with other members of the ASO technical development team.Responsibilities* Evaluating drug delivery platforms and developing manufacturing processes to support animal and clinical studies* Supporting ASO fill-finish process development work at with external vendors and contract manufacturing sites for delivery systems and parenteral drug product formulations* Conducting bench scale studies to develop ASO drug delivery systems including formulation, purification and analytic development* Execution of ASO formulation and process development study protocols, stability and product characterization studies* Closely interfacing with chemical synthesis, purification and analytic groups to support ASO manufacturing platforms* Authoring and reviewing all necessary SOPs, protocols, and study reports* Presenting scientific data to technical teams, ability to manage several projects simultaneously, and excellent communication skills, both written and oral.*LI-POT6Qualifications* Experience in developing and analyzing drug delivery systems, such as microspheres and liposomes, including the generation of material suitable for animal and human studies* Understanding of drug product manufacturing process operations such as mixing, sterile filtration, extractable/leachable assessments and container filling/closing.* Sound knowledge of formulation development and stabilization of therapeutics, preferably with hands-on experience with oligonucleotides and delivery systems* Experience in analytical and characterization methods such as chromatography, spectroscopy, calorimetry and particle analysis technologies* Use of membrane technologies for preparing formulations, experience with aseptic technique for stability and preclinical material preparation* Prior experience working in a biopharmaceutical product development environment and familiarity with GMPs and FDA/ICH guidelines is preferred.EducationPhD in Pharmaceutical Sciences, Biochemical or Chemical Engineering, or related discipline, with 2+ years of industrial experience or BS/MS with 8+ years of related industrial experience.All 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
Scientist I / II, Drug Product Delivery, Antisense Oligonucleotide (AS
SummaryAs a member of Biogen's Antisense Oligonucleotide Drug Product development team, the candidate will dive a cross-functional team evaluating antisense oligonucleotide (ASO) drug delivery platforms.Job DescriptionThe candidate will be responsible for formulation and process development activities of ASO drug product development programs. Conducting in-house laboratory studies and managing technical work with manufacturing facilities is a requirement of the position. Candidate is expected to work collaboratively in a matrix environment with other members of the ASO technical development team.Responsibilities* Evaluating drug delivery platforms and developing manufacturing processes to support animal and clinical studies* Supporting ASO fill-finish process development work at with external vendors and contract manufacturing sites for delivery systems and parenteral drug product formulations* Conducting bench scale studies to develop ASO drug delivery systems including formulation, purification and analytic development* Execution of ASO formulation and process development study protocols, stability and product characterization studies* Closely interfacing with chemical synthesis, purification and analytic groups to support ASO manufacturing platforms* Authoring and reviewing all necessary SOPs, protocols, and study reports* Presenting scientific data to technical teams, ability to manage several projects simultaneously, and excellent communication skills, both written and oral.*LI-POT6Qualifications* Experience in developing and analyzing drug delivery systems, such as microspheres and liposomes, including the generation of material suitable for animal and human studies* Understanding of drug product manufacturing process operations such as mixing, sterile filtration, extractable/leachable assessments and container filling/closing.* Sound knowledge of formulation development and stabilization of therapeutics, preferably with hands-on experience with oligonucleotides and delivery systems* Experience in analytical and characterization methods such as chromatography, spectroscopy, calorimetry and particle analysis technologies* Use of membrane technologies for preparing formulations, experience with aseptic technique for stability and preclinical material preparation* Prior experience working in a biopharmaceutical product development environment and familiarity with GMPs and FDA/ICH guidelines is preferred.EducationPhD in Pharmaceutical Sciences, Biochemical or Chemical Engineering, or related discipline, with 2+ years of industrial experience or BS/MS with 8+ years of related industrial experience.All 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
Manager, Regulatory Affairs
SummaryThe Manager, Regulatory Affairs manage ex-US Clinical Trial Application (CTA) submissions to national competent authorities (NCAs) to include initial submissions, amendments, and notifications. Responsible for accuracy and content of submissions and communications with regulatory agencies that are compliant with agency regulations. Analysis of regulatory issues and guidelines related to clinical trials.Job DescriptionKey Responsibilities:* Perform the following functions (with oversite) required to manage clinical trial applications for 2-4 Programs:* Act as the regulatory contact with the Clinical Research Organization (CRO)* Liaise with Global Clinical Operations (GCO), the Global Regulatory Lead (GRL) and the Clinical Research Organization (CRO) to establish a global submission plan for clinical trials* Coordinate and prepare with CRO or BIIB Affiliate the global regulatory clinical trial applications (CTAs) including initial CTAs, amendments, and notifications up through CSR.* Identify and communicate a final list of country requirements and potential challenges with assistance of the CRO* Facilitate query management and the finalization and submission of responses to NCAs* Provide regular CTA status updates to the GRL* Represent the Regulatory Project Team (RPT) at Study Management Team (SMT) meetings* Gather and distribute regulatory intelligence to the CTA Team* Collaborate with groups both within the Regulatory Affairs department and across the organization as a whole to promote transparency and communication* Highlight regulatory trends related to clinical trial applications to the department and teams to allow for appropriate planning and to minimize impactQualifications* 3-5 years in industry (at least 1-2 years in regulatory) preferred* Good knowledge and understanding of regulations/ability to interpret regulations * Understanding and knowledge of CTA Regulations (e.g., EU CT-1)* Ability to multi-task and work independently* Strong communication skills and the ability to influence without authority* Ability to work effectively under pressure* Strong organizational skills to effectively manage complex issues while maintaining dynamic timelines.EducationBA/BS/University degree required, Life/Health Sciences preferred.All 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
Manager, Regulatory Affairs
SummaryThe Manager, Regulatory Affairs manage ex-US Clinical Trial Application (CTA) submissions to national competent authorities (NCAs) to include initial submissions, amendments, and notifications. Responsible for accuracy and content of submissions and communications with regulatory agencies that are compliant with agency regulations. Analysis of regulatory issues and guidelines related to clinical trials.Job DescriptionKey Responsibilities:* Perform the following functions (with oversite) required to manage clinical trial applications for 2-4 Programs:* Act as the regulatory contact with the Clinical Research Organization (CRO)* Liaise with Global Clinical Operations (GCO), the Global Regulatory Lead (GRL) and the Clinical Research Organization (CRO) to establish a global submission plan for clinical trials* Coordinate and prepare with CRO or BIIB Affiliate the global regulatory clinical trial applications (CTAs) including initial CTAs, amendments, and notifications up through CSR.* Identify and communicate a final list of country requirements and potential challenges with assistance of the CRO* Facilitate query management and the finalization and submission of responses to NCAs* Provide regular CTA status updates to the GRL* Represent the Regulatory Project Team (RPT) at Study Management Team (SMT) meetings* Gather and distribute regulatory intelligence to the CTA Team* Collaborate with groups both within the Regulatory Affairs department and across the organization as a whole to promote transparency and communication* Highlight regulatory trends related to clinical trial applications to the department and teams to allow for appropriate planning and to minimize impactQualifications* 3-5 years in industry (at least 1-2 years in regulatory) preferred* Good knowledge and understanding of regulations/ability to interpret regulations * Understanding and knowledge of CTA Regulations (e.g., EU CT-1)* Ability to multi-task and work independently* Strong communication skills and the ability to influence without authority* Ability to work effectively under pressure* Strong organizational skills to effectively manage complex issues while maintaining dynamic timelines.EducationBA/BS/University degree required, Life/Health Sciences preferred.All 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
Scientist I, Biomedical Informatics
SummaryWe are seeking a talented scientist in biomedical informatics to develop and apply statistical and machine learning methods to large-scale clinical and molecular profiling datasets to drive drug discovery and translational medicine in neurodegenerative and neuroinflammatory disorders.Job DescriptionIntegrative analysis of clinical, imaging and molecular (genetics, transcriptomics, proteomics, metabolomics, microbiome) data from multiple patient cohorts and studies is key to providing molecular-level insights into disease risk, heterogeneity and progression as well as identifying clinically relevant subgroups for novel drug and biomarker discovery and clinical trial design. As a member of the Translational Integrative Analytics group, the successful candidate will perform integration of high-dimensional data from public databases, internal cohorts and patient registries, using statistical analysis, machine learning and knowledge-graphs to generate hypothesis about causal pathways and to develop clinical decision tools for patient stratification. The scientist will work cross-functionally with computational systems biologists, therapeutic area research scientists, translational science and clinical teams and will engage with the external research community to further our understanding of neurological diseases at a molecular level and to drive innovation in computational tools for drug development.QualificationsThorough understanding of molecular biology and profiling technologies (whole-exome sequencing, bulk tissue and single-cell RNA-seq, targeted proteomics platforms, immunophenotyping) and demonstrated ability to design experiments and execute data collection, QC and analysis plans using these technologies in a disease context is required.* Expertise in developing, using or adapting open-source tools in R and python for normalization, exploration and analysis of high-dimensional data (NGS, proteomics). Understanding of best practices in code, data-management and sharing is required. Experience with clinical data standards and analysis of electronic health record data is desired.* Familiarity with modern computing environments (HPC, AWS) as well as deep expertise in one or more of statistical learning, signal processing, Bayesian analysis, network biology, machine learning or deep learning domains is required. * Excellent communication and presentation skills are required. Proven ability to work independently in complex and dynamic project oriented team settings and a record of delivering consistent and high-quality results is required.* Experience with neurology or immunology is desirable but not required.EducationPh.D. in a quantitative scientific discipline such as computer science, bioinformatics, systems biology, physics or engineering. 2+ years of experience with working with cross-functional teams preferably in industry or drug-discovery settingAll 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
Scientist I, Biomedical Informatics
SummaryWe are seeking a talented scientist in biomedical informatics to develop and apply statistical and machine learning methods to large-scale clinical and molecular profiling datasets to drive drug discovery and translational medicine in neurodegenerative and neuroinflammatory disorders.Job DescriptionIntegrative analysis of clinical, imaging and molecular (genetics, transcriptomics, proteomics, metabolomics, microbiome) data from multiple patient cohorts and studies is key to providing molecular-level insights into disease risk, heterogeneity and progression as well as identifying clinically relevant subgroups for novel drug and biomarker discovery and clinical trial design. As a member of the Translational Integrative Analytics group, the successful candidate will perform integration of high-dimensional data from public databases, internal cohorts and patient registries, using statistical analysis, machine learning and knowledge-graphs to generate hypothesis about causal pathways and to develop clinical decision tools for patient stratification. The scientist will work cross-functionally with computational systems biologists, therapeutic area research scientists, translational science and clinical teams and will engage with the external research community to further our understanding of neurological diseases at a molecular level and to drive innovation in computational tools for drug development.QualificationsThorough understanding of molecular biology and profiling technologies (whole-exome sequencing, bulk tissue and single-cell RNA-seq, targeted proteomics platforms, immunophenotyping) and demonstrated ability to design experiments and execute data collection, QC and analysis plans using these technologies in a disease context is required.* Expertise in developing, using or adapting open-source tools in R and python for normalization, exploration and analysis of high-dimensional data (NGS, proteomics). Understanding of best practices in code, data-management and sharing is required. Experience with clinical data standards and analysis of electronic health record data is desired.* Familiarity with modern computing environments (HPC, AWS) as well as deep expertise in one or more of statistical learning, signal processing, Bayesian analysis, network biology, machine learning or deep learning domains is required. * Excellent communication and presentation skills are required. Proven ability to work independently in complex and dynamic project oriented team settings and a record of delivering consistent and high-quality results is required.* Experience with neurology or immunology is desirable but not required.EducationPh.D. in a quantitative scientific discipline such as computer science, bioinformatics, systems biology, physics or engineering. 2+ years of experience with working with cross-functional teams preferably in industry or drug-discovery settingAll 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
See More