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Hims & Hers is hiring a VP of R&D and Innovation to lead end-to-end product innovation, scale scientific discoveries into commercial products, and establish robust R&D infrastructure across regulated compounding environments.

Senior QA leader needed to establish and scale a combination-product Quality Assurance function for a clinical-stage biotech developing biologics and autoinjector-enabled therapies.

Senior CMC Program Officer to lead strategic and technical CMC guidance for vaccine development targeting polio eradication and other global health priorities at a leading nonprofit foundation.

Senior scientific leader needed to direct global biologics formulation development and technology transfer activities across multiple sites to advance veterinary pharmaceutical and vaccine products to market.

Lead the global regulatory strategy and submissions for a growing clinical-stage biotech developing innovative autoimmune therapies, serving as the regulatory lead for the MMN program (remote, U.S.).

Strategically lead and manage drug and drug–device development for the Women’s Health Innovations team, driving portfolio decisions, partnerships, and clinical advancement of contraceptive and STI therapeutics.

AbbVie is hiring a Principal Scientist in Formulation Development to lead late-stage oral solid formulation, scale-up, tech transfer, and CMC submissions for clinical and commercial programs.

Experienced QA professional needed to lead and coordinate Annual Product Reviews and quality trending for small-molecule commercial products at Vertex in a six-month contract assignment.

Lead regulatory strategy and thought leadership for biologics and cell & gene therapy programs at a science-driven consultancy advising biotech and healthtech innovators worldwide.

Bristol Myers Squibb is hiring an Associate Director / Director to lead global drug product lifecycle strategy and execution for cell therapy manufacturing at the Summit West site.

Lead and scale Conception’s iPSC core to deliver reliable, traceable cell culture operations and QC systems that enable R&D through CMC readiness.

Lead and grow the Analytical Sciences function at Editas to establish robust analytical control strategies, methods, and specifications for in‑vivo gene‑editing programs.

Senior Program Officer to lead and manage a high-impact regulatory affairs portfolio, supporting WHO, EMA, and AMA partnerships to strengthen global and African regulatory systems for medical products.

Moderna seeks an Associate Director in CMC for its 18-month MBA Accelerator program to lead strategic, cross-functional projects and accelerate into enterprise leadership.

Eurofins is hiring a Particulates Lab Associate to perform and document particulate testing and analytical method support on-site in Boston for pharmaceutical CMC projects.

Moderna seeks a Senior Manager, Analytical Science & Technology (AS&T) to lead analytical method qualification, validation, transfer, and lifecycle strategy for late‑phase and commercial CMC programs at the Norwood, MA site.

Experienced analytical chemist needed to lead LC‑MS-based method development and impurity characterization for late-stage CMC development at a major biopharmaceutical company in North Chicago, IL.

AbbVie is hiring an experienced analytical chemist to lead LC‑MS-based analytical development and impurity characterization for late-stage drug substance and drug product programs.

Lead development and implementation of data-rich, automated in-process analytical methods to accelerate cell line and process development for complex biologic therapies at AbbVie's South San Francisco biologics CMC team.

AbbVie seeks an experienced CMC leader to direct global dossier strategy and coordinate cross-functional teams to produce high-quality regulatory submissions for small-molecule programs.

Experienced CMC biologics program leader needed to drive process development, regulatory strategy, and cross-functional delivery for AbbVie's biologics pipeline.

Lead global drug product development and CDMO operations at Dyne Therapeutics to ensure reliable clinical supply and commercial launch readiness for injectable therapeutics.

AbbVie's Biologics Drug Product Development team is looking for a PhD student intern to study LLPS and excipient-driven colloidal stability in high-concentration biologic formulations at the South San Francisco CMC site.

PhD-level Drug Substance intern to support cell line engineering, mammalian cell culture, and protein purification efforts within AbbVie's BioCMC team in South San Francisco.

Vertex is hiring a hybrid contract Project Manager with CDMO and tech-transfer experience to lead cross-functional CMC projects supporting cell and gene therapy development.

Lead analytical science and commercial strategy for biologics and advanced therapies in North America as SGS's Head of Pharma Science.

Lead the Analytical Technologies effort within BMS Cell Therapy Analytical Development to streamline assay workflows, implement automation, and speed product development.

Experienced CMC leader sought to drive global product development strategy, lead cross-functional teams, and ensure regulatory-ready CMC deliverables for AbbVie's development portfolio.

Lead CMC dossier planning and coordination at AbbVie’s North Chicago site to drive timely, high-quality regulatory submissions and cross-functional alignment.

Lead CMC dossier planning and coordination at AbbVie to ensure timely, high-quality regulatory submission deliverables across late-stage development projects.

A lab-facing Senior Scientist role at AbbVie South San Francisco to execute CMC data digitization, integrate ELN/LIMS/SDMS and enable workflow automation supporting biologics development.

Lead and build clinical and commercial supply chain strategy and operations at ORIC to ensure compliant, cost-effective delivery of investigational and commercial drug product across global trials and launch readiness.

Experienced CMC regulatory professional needed to lead global regulatory strategies and submissions for small-molecule drug development at AbbVie’s North Chicago hybrid site.

Lead technical evaluations, due diligence and deal execution for licensing and acquisition opportunities within AbbVie's PDS&T organization to support strategic growth.

Lead global industrialization programs at AbbVie, providing strategic program management and cross-functional leadership to ensure successful transfer and commercialization of biologics and combination products.

Senior regulatory leader needed to lead global regulatory strategy and submissions for DiaMedica’s biologics pipeline, interfacing with FDA and other global agencies.

Landmark Bio is hiring a Director, CMC Technology & Innovation Program Lead to spearhead continuous biomanufacturing innovation and deliver connected GMP manufacturing solutions for advanced therapeutics.

TetraScience is hiring a Scientific Data Architect in the Boston region to design reusable scientific data models, implement cloud-based pipelines and integrations, and deliver AI-enabled outcomes for biopharma customers.