Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP)
$241k - $332kBiogen Idec
About This Role:As the Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP), you will lead a dynamic team within the PO&T function, driving the regulatory strategy for biologics and ATMPs in Biogen’s portfolio. Your role encompasses global, regional, and local accountability for all therapeutic areas relevant to these modalities. You will manage resources, set a vision, and ensure alignment between regulatory strategy, technical development, and manufacturing execution. By leading multiple projects in a fast-paced environment, you will play a crucial role in delivering on our product portfolio, providing strategic oversight to ensure timely approvals and lifecycle progression. Your leadership will be pivotal in fostering collaboration across the company, aligning regulatory strategies with manufacturing readiness and supply continuity.This is a hybrid role to be based at our Headquarters in Cambridge, MA.What You’ll Do:Lead the CMC regulatory team in the development and execution of global CMC regulatory strategies for biologics and ATMPs.Assess regulatory risks and develop mitigation approaches to support timely product approvals.Ensure submission readiness and regulatory compliance across all phases of development and commercialization.Guide global interactions with Health Authorities for CMC topics, preparing briefing materials and responses to agency questions.Provide oversight for post-approval lifecycle activities, evaluating manufacturing and analytical changes for regulatory submissions.Represent the regulatory function in evaluating new product opportunities, coordinating with Technical Operations, Quality, and Supply Chain.Participate in external industry meetings and forums, organizing discussions and delivering presentations.Offer recommendations and risk assessments to influence decision-making in governance forums.Review and approve regulatory submissions ensuring alignment with global requirements and business timelines.Who You Are:You are a visionary leader with a deep understanding of regulatory sciences, skilled at navigating the complexities of biologics and ATMPs. Your strategic mindset and collaborative spirit enable you to forge strong partnerships across functions and drive innovative solutions. With your exceptional communication and problem-solving skills, you inspire confidence in stakeholders and lead your team to achieve ambitious goals. Your passion for regulatory excellence and dedication to advancing therapeutic solutions make you a vital asset to our organization.Required Skills:Advanced Degree or Ph.D. in Life Sciences, Pharmacy, Medicines, or related discipline.Minimum of 15 years of experience within regulatory agencies or the Pharmaceutical Industry.Significant leadership experience in Regulatory Sciences.Proven track record of successful global regulatory submissions and approvals for biologics and/or ATMPs.Significant understanding of international regulations and policy-setting processes of major regulatory agencies.Active engagement in major industry associations, conferences and forums.Strong collaboration and negotiation skills with cross-functional teams.Experience working across global development and manufacturing networks, including external partners.Job Level: ManagementAdditional InformationThe base compensation range for this role is: $241,000.00-$332,000.00Base salary offered is determined through an analytical approach utilizing a combination of factors including, but not limited to, relevant skills & experience, job location, and internal equity.Regular employees are eligible to receive both short term and long-term incentives, including cash bonus and equity incentive opportunities, designed to reward recent achievements and recognize your future potential based on individual, business unit and company performance. In addition to compensation, Biogen offers a full and highly competitive range of benefits designed to support our employees’ and their families physical, financial, emotional, and social well-being; including, but not limited to:Medical, Dental, Vision, & Life insurancesFitness & Wellness programs including a fitness reimbursement Short- and Long-Term Disability insuranceA minimum of 15 days of paid vacation and an additional end-of-year shutdown time off (Dec 26-Dec 31)Up to 12 company paid holidays + 3 paid days off for Personal Significance 80 hours of sick time per calendar yearPaid Maternity and Parental Leave benefit 401(k) program participation with company matched contributionsEmployee stock purchase plan Tuition reimbursement of up to $10,000 per calendar year Employee Resource Groups participationWhy 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 Biogen.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.SummaryLocation: Cambridge, MAType: Full time
$163.5k - $281.6k
...life-changing medicines, strengthen how... ...Director, Regulatory CMC to lead and execute... ...-edge gene therapy portfolio. This... ...throughout the product lifecycle.... ...therapies and advanced therapeutic medicinal... ...products (ATMPs).Lead and mentor... ..., Molecular Biology, Chemistry, Pharmacy...SuggestedFor contractorsWork at officeFlexible hours$238k - $374k
...innovation and delivers transformative therapies to patients. By focusing R&D... ...As Executive Director, Global Regulatory Affairs CMC Devices and Drug-Device Combination Product, you will provide strategic... ...Requirements/Qualifications: Advanced degree in a scientific, or...SuggestedMinimum wageTemporary workWork at officeLocal areaRemote workWorldwide$190.4k - $285.6k
...Manufacturing Controls (CMC) leads a Regulatory CMC team... ...and commercial products in the small molecule... ...up to date on advances in technology,... ...Degree in Chemistry, Biology, Pharmacy,... ...transformative medicines for people with... ...investigational therapies across a range of...SuggestedSummer workRemote workFlexible hours2 days per week$182k - $275k
...diseases. We develop medicines for previously untreatable... ...based, and compliant regulatory CMC deliverables for... ...regulatory programs for products intended to treat... ...diseases by rapidly advancing care and precision medicines... ...and developing novel therapies for other rare...SuggestedWork at office$170k - $220k
Associate Director, Regulatory CMC - Solid... ...precision genetic medicine company focused on advancing a portfolio of gene therapy candidates targeting... ...will report to Head of Regulatory CMC... ...and refine the product development strategy... ...CMC aspects of biological product...SuggestedFull timeTemporary workRemote workFlexible hours$166.4k - $249.6k
...Chemistry Manufacturing Controls (CMC) Associate Director leads and executes global regulatory CMC strategies across investigational and commercial products focusing on biologics. This role is accountable for... .... The role integrates advanced digital and AI-enabled approaches...Full timeSummer workRemote workFlexible hours2 days per week$238k - $374k
...and delivers transformative therapies to patients. By focusing R... ...Director, Global Regulatory Affairs CMC Early Development you will... ...strategies for small molecule and biologic products for FIH to pre‑pivotal... ...functional decision‑making, and advancing adoption of in silico and...Full timeTemporary workLocal areaWorldwide$218.06k - $327.09k
...Senior Director, Regulatory Affairs Strategy - Cell Therapy Available... ...closely with Global Product Teams to align... ...with clinical, CMC, safety and commercial... ...that advance how we work and... ...of overall drug/biologic development processes... ...life-changing medicines. In-person...Hourly payFull timeTemporary workStart working todayWork at officeFlexible hours3 days per week$177k - $278.08k
...delivers transformative therapies to patients. By... ...is within the Global Regulatory Affairs (GRA) Chemistry... ...Manufacturing & Controls (CMC) and Devices organization... ...for their assigned product(s) and may serve as the... ...Scientific Discipline, Advanced Degree (M.S., Ph.D.,...Minimum wageTemporary workLocal areaRemote workWorldwide- ...deliver innovative medicines and solutions... ...- and products and services in... ...Senior Manager Regulatory Affairs, Chemistry... ...and Controls (CMC) works with... ...patients to deliver biologics products to... ...cell & gene therapies. Prepares CMC... ...Education: Relevant advanced degree...Work at officeLocal areaRemote work
$204k - $245k
...that’s pursuing curative gene therapies to give patients and their... ...radical care. The Director, Regulatory CMC is responsible for leading execution... ...and late‑stage gene therapy products, with a primary focus on... ...(biochemistry, chemistry, biology, biochemical engineering, or...Full timeWork at officeFlexible hours3 days per week$242k - $313.5k
...About Beeline Medicines: Beeline Medicines is a... ...‑leading precision therapies to transform the lives... ...Senior Director, Regulatory Affairs CMC – Biologics provides senior‑level... ...for biological products. As a senior leader... ...Qualifications Education: Advanced degree (PhD, MS, or...Local areaFlexible hours2 days per week$200k - $220k
...Senior Director, Regulatory CMC Join Us in Tackling... ...of disease. By advancing telitacicept, a first... ...working on a medicine. You’re part of a... ...one indication – a therapy that has already... ...development of biologics and combination biologic/device products is a must. Key Areas...Contract workWorldwideFlexible hours$290k - $323k
...bringing the next wave of therapies for cancer patients.... ...aims to rapidly advance potentially transformative... .../or oversee global regulatory CMC submissions (e.g.,... ..., MAAs etc.) through product lifecycle. Proactively... ...drug conjugates and biologics Strong analytical, strategic...Temporary workFor contractorsFlexible hours$212k - $333.19k
...and delivers transformative therapies to patients. By focusing R... ...As Senior Director and Regulatory Platform Lead GRA CMC, Device and Drug‑Device Combinations... ...device and combination product regulatory strategies,... ...Engineering Discipline, Advanced Degree Preferred. 10+ years...Full timeTemporary workLocal areaWorldwideNight shift$268.2k - $402.2k
...The Executive Director, Regulatory Strategy will serve as... ...knowledge and advanced drug development expertise... ...regulatory strategies for product development and... ...pharmaceutical development of medicines for human use.... ...:Bachelor's degree in Biology, Chemistry, or other related...Full timeSummer workLocal areaRemote workFlexible hours2 days per week$212k - $333.19k
...transformative therapies to patients.... ...vision, we are advancing a rapidly growing... ...), complex biologics and small molecules... ...medicines and make a lasting... ...Director, Global Regulatory Lead - Oncology... ...access of our products to patientsWill... ...Lead and/or TA Head. May...Minimum wageTemporary workLocal areaRemote workWorldwide$224.9k - $404.6k
...managing a team of CMC experts that... ...correspondence and regulatory applications. This... ...required to oversee the product strategy for all... ...degree in Molecular Biology, Pharmaceutics,... ...to reimagine how medicines are created and delivered... ..., developing, and advancing our employees. By...Permanent employmentFull timeWork at officeWork from home- ...CF by developing novel medicines that normalize the... ...NBD1, the company is advancing a pipeline of novel small... ...work closely with the CMC, Quality Assurance, Clinical... ...Drug Supply, and Regulatory Affairs teams to ensure... ...leadership across the product lifecycle, from...Flexible hours
$163.5k - $281.6k
...life-changing medicines, strengthen how... ...global regulatory CMC strategies for... ...assigned gene therapy programs, including... ...throughout the product lifecycle. Proactively... ...therapies and advanced therapeutic... ...products (ATMPs). Lead and... ...Biochemistry, Molecular Biology, Chemistry,...Full timeFor contractorsWork at officeFlexible hours$220k - $290k
...Verastem Oncology, we’re advancing innovation and... ...the first therapy specifically for women... ...and are exploring regulatory pathways for Europe... ...of investigational products and guide and... ...supports product (drugs, biologics and devices)... ...development program. Guide CMC, nonclinical and...Temporary workFor contractorsWork at officeWeekday work$170.9k - $231.3k
## Associate Director, Regulatory Affairs, CMCUnited... ...Director, Regulatory Affairs CMC Development is... ...scientific foundation in biologics and/or complex modalities... ...strategic guidance on product characterization,... ...capability.**Qualifications*** Advanced degree in chemistry,...Full timeTemporary workWork at officeLocal areaFlexible hours$276k - $414k
...Title: Executive Director, Regulatory Affairs Strategy - Cell Therapy Available locations:... ...turn science into approved medicines? Do you see yourself steering... ..., define target product labeling, and accelerate... ...experience of overall drug/biologic development processes and...Hourly payFull timeTemporary workWork at officeWorldwideFlexible hours3 days per week$180k - $270k
...market dynamics, regulatory requirements, emerging... ...outcomes. Product Support– Proactively... ...transformative medicines for people with serious... ...and continues to advance clinical and... ...investigational therapies across a range of... ...into causal human biology, including APOL1‑...Long term contractContract workSummer workWork at officeRemote workFlexible hours2 days per week$160k - $240k
...degradation (TPD) to develop medicines that address critical... ...therapeutics. Having advanced the first degrader... ..., highly effective therapies for patients with these... ...Medicine, Research, and/or CMC.Demonstrated ability... ...to build and maintain productive relationships with...Contract work$196k - $240k
...disease. The company is advancing clinical programs... ...The Director, Regulatory Affairs –... ...Manufacturing, and Controls (CMC) is responsible... ...through and beyond product approval. This... ...leading CMC sections of biologics marketing... ...the advancement of therapies for patients with...Local areaWorldwide$159k - $195k
Department: 1310US - Regulatory - USLocation: Waltham,... ...disease. The company is advancing clinical programs for... ...Manufacturing and Control (CMC) is accountable for... ...pertaining to global product development... ...developing CMC sections of Biologics marketing applications...Local area- ...Director, Global Regulatory Affairs... ...across the full product lifecycle, from... ...oncology drug and biologic development, strong... ..., breakthrough therapy designation,... ...Clinical Operations, CMC/Technical... ...discipline required; advanced scientific... ...to delivering medicines that provide a...
$281k - $344k
...About Beeline Medicines Beeline Medicines is a clinical... ...‑leading precision therapies to transform the lives... ...The Executive Director, Regulatory Affairs will report to... ...regulatory strategy for the product, ensuring timely... ...assigned. Qualifications Advanced degree (PhD, PharmD,...For contractorsLocal areaFlexible hours2 days per week$150k - $180k
...ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.At Cytiva you will be able... .../or territory/region on products or services. Establishes... ...business problems by applying advanced critical thinking—...Full timeRemote workNight shift
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Head of Regulatory CMC - Biologics & Advanced Therapy Medicinal Products (ATMP). Be the first to apply!
- regulatory affairs manager pharmaceutical Cambridge, MA
- manager regulatory affairs Cambridge, MA
- regulatory manager Cambridge, MA
- compliance manager Cambridge, MA
- compliance director Cambridge, MA
- director global regulatory affairs Cambridge, MA
- regulatory & compliance manager Cambridge, MA
- regulatory affairs director Cambridge, MA
- head compliance Cambridge, MA
- food regulatory Cambridge, MA



