CMC Program Director, Drug Substance
$210k - $240kCentessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company
Centessa Pharmaceuticals in Boston seeks a Director for CMC Program Management. The role involves leading operational support for drug substance development and ensuring effective execution of project deliverables in collaboration with internal teams and external partners. Ideal candidates have over 10 years of experience in the pharmaceutical industry, particularly in small molecule development. This full-time position offers a base salary of $210,000 to $240,000, plus bonuses and comprehensive benefits. #J-18808-Ljbffr Centessa Pharmaceuticals, a wholly owned subsidiary of Eli Lilly and Company
$150k - $211k
Role Summary Reporting to the Director of Drug Substance (Biologics), MSAT, this role is an individual... ...analyze process trends and control charts. CMC & Regulatory Support Author and review... ...short‑term and long‑term incentive programs. Servier also offers a competitive and...SuggestedTemporary workRemote workFlexible hours- Zealand Pharma seeks a Global Head of Drug Substance - Senior Director in Boston to build and lead a new peptide process development function from the ground up, establishing a state‑of‑the‑art lab and team while providing global leadership across Drug Substance. You will...Suggested
- Centessa Pharmaceuticals in Boston is seeking an Associate Director for Small Molecule Drug Substance Process Chemistry. The candidate will coordinate with CDMOs to manage production of chemical intermediates and APIs for research and clinical studies. The ideal candidate...Suggested
- ...portfolio of differentiated programs that are designed to harness... ...of approved oligonucleotide drugs. Korro is based in Cambridge... ...health. Position Summary The Director, CMC QA will be responsible for... ...vendors to ensure that drug substance, drug product, and finished...Suggested
- Takeda in Boston, MA seeks a Director of Regulatory Site CMC to lead post‑approval change management across multiple sites, guiding submissions and... ...regulatory activities. You will communicate regulatory strategy to drug development, registration, and post‑market teams,...Suggested
$170k - $220k
...Associate Director, Regulatory CMC – Solid Biosciences Charlestown, MA HQ Solid Biosciences is a precision... ...the forefront of development of our programs and regulatory CMC provides a... ...regulatory CMC experience in gene therapy drug development. The candidate will play an...Full timeTemporary workRemote workFlexible hours$235k - $285k
...patient experience and building the future of drug delivery. We are passionate about the... ...thrive. Join us as a Senior Director, CMC Technical Lead , and you’ll be part of a... ...experienced CMC Technical Lead to join our Program Management and Portfolio Strategy team....Temporary workLocal area$293k - $358k
...is looking for a Vice President of Technical Operations to lead CMC strategy. This strategic role involves building a high-performing... ...successful candidate will have deep expertise in small molecule drug development and will collaborate with Regulatory Affairs and Quality...- EyePoint is seeking a hybrid-eligible CMC/Technical Operations professional in Watertown, MA, to drive late-stage development activities and NDA readiness. The role coordinates manufacturing readiness, process development, and cross-functional governance to ensure on-time...Contract work
$200k - $270k
...Job Description Description: Associate Director/Director Drug Product and Formulation Development At... ...studies as appropriate. Work closely with CMC colleagues to ensure consistent manufacturing timelines across drug substance, drug product, and QA/QC. Author...Contract workLocal area- Genepool Networks in Boston is seeking a Senior Director of Program Management to lead cross-functional development programs from late discovery... ...&D functions. An understanding of regulatory submissions and drug development is essential. Ideal candidates have prior...
$214k - $249.8k
...address significant unmet needs. The Director, Head of Drug Product Analytical Operations leads analytical... ...products, and related packaging within CMC activities. The role provides strategic... ...oversees outsourced analytical programs, drives risk-based decisions, ensures compliance...- ...potential of genetic medicine, Landmark Bio offers deep drug development expertise and integrated end-to-end... ...therapies. We are seeking an experienced and visionary Director, CMC Technology & Innovation Program Lead to drive the development of next-generation biomanufacturing...
- ...stage radiopharmaceutical company is looking for a Manager of Quality Operations to oversee quality assurance systems and support the CMC activities. The role requires at least 5 years of quality assurance experience in the pharmaceutical industry and expertise in GMP...Full time
- The Role: Reporting to the Exe. Director of Digital Operations and Strategic Portfolio Management... ...and aligning operations within Moderna’s CMC Digital organization and TPM for cross-... ...design and orchestration of digital programs that enable transformational CMC capabilities...Permanent employment
- ...MA seeks an experienced sales professional to identify, qualify and close opportunities in industrial and academic accounts for our drug discovery products. You will provide field-based technical introductions, conduct on-site seminars and demos, and support marketing...
- A global healthcare leader in Boston seeks a Senior Director for Drug Delivery Technologies. This role involves leading strategic projects in drug delivery, collaborating across teams, and leveraging scientific principles for improving clinical outcomes. The ideal candidate...
$300 per month
...nurturing your professional growth and success. Regional Technical Program Manager Role: As a member of the company’s Data Center... ...completion of a background check and, where permitted by law, a 5‑panel drug test conducted after the offer letter is signed, which will...Full timeTemporary workWork at officeImmediate startVisa sponsorshipWork visaFlexible hours2 days per week- Director/Associate Director, Cell Therapy CMC & Manufacturing We are seeking a highly experienced and visionary leader of CMC & Manufacturing to lead our cell therapy development programs. The successful candidate will help lead CMC strategy, manage process development...
$311k - $388.5k
...differentiated by radically more efficient drug development. Advancements in AI and drug... ...research organizations, and biotechs to develop programs past clinical proof of concept and beyond,... ...functional subject matter experts (e.g., CMC, Regulatory, Data Science) to drive asset...Full timeContract workWork at officeLocal areaRelocationFlexible hours3 days per week- .... While nearly every antibody drug works by blocking an overactive... ...model cannot. Our lead program, DIAG723, is the first clustering... ...highly motivated and strategic Director, Program Management, to drive... ...Operations, Regulatory Affairs, CMC, Research, Translational Sciences...Local area
$196k - $240k
...experiences to join our team. What You’ll Do The Director, Program Management will collaborate with cross‑... ...candidate must have experience managing drug development projects in a fast‑paced... ..., regulatory, and technical operations/CMC - and an understanding of how these...Full timeLocal areaFlexible hours3 days per week$159k - $195k
...Role Summary The Associate Director, Regulatory Chemistry Manufacturing and Control (CMC) is accountable for executing global... ...CMC regulatory strategies for our programs in early and late-stage... ...filings Thorough understanding of drug development process and the pharmaceutical...Local area- ...develop & advocate strategic positions for CMC regulatory/CMC issues with cross... ...content consistency and best practices across programs. ~ Advocate with regulatory agencies, industry... ...(as described above) including: ~Drug Development/CMC experience is most relevant...Local area
$138.7k - $208.1k
...seeking a Senior Manager for Manufacturing Science & Technology in Boston, MA. This role provides technical leadership for sterile drug product manufacturing processes in both clinical and commercial settings. The manager will oversee process transfers, validations, and...$238k - $374k
...a dedicated group of experienced biologic drug hunters within AIRx that has the autonomy... ...success rates. About the Role As AIRx Biologics Program Lead, you will own the end‑to‑end... ...candidates based on scientific, clinical, CMC, and commercial considerations; balance potency...Minimum wageTemporary workLocal areaRemote work$140k - $165k
...needs. Science and Technology (SAT) is part of the Global CMC, Science & Technology Department (GCSAT). GCSAT is responsible... ...Responsibilities: Subject matter expert (SME) for Small Molecules Drug Substance Manufacturing. Process owner of Small Molecules process...Contract workTemporary work- ...Description Job Description As a Clinical Residential Program Director for North Suffolk Community Services, you’ll be in charge of... ...rehabilitation. Assist people with psychiatric and substance use disorders to identify personal priorities, preferences,...Temporary workFlexible hours
$152.6k - $283.4k
...seeking an accomplished Associate Director to join our discovery... ...advancing differentiated antibody-drug conjugates (ADCs) and related... ...conjugation expertise to therapeutic program strategy. You will collaborate... ..., translational sciences, and CMC teams to advance next-...- ...What You Will Do The Global Safety Program Lead, Senior Director is accountable to the Global Safety Head for the safety strategy, delivery, and... ...leaves; and, health benefits including medical, prescription drug, dental, and vision coverage in accordance with the terms...Hourly payTemporary workLocal area
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