Cdmo Jobs

Amylyx is hiring an Associate Director, Drug Substance to lead technical development, scale-up, and regulatory CMC activities for peptide and oligonucleotide drug substances while collaborating with CDMOs and cross-functional teams.

Lead small-molecule drug substance process development and CDMO management for a publicly traded biotech advancing registration-directed clinical programs.

Terremoto Biosciences is hiring an experienced Director/Sr. Director to lead analytical development and QC for small molecule programs, overseeing internal activities and CDMO partnerships in South San Francisco.

Senior Director, Manufacturing to lead end-to-end bioprocess operations and manufacturing teams at KBI Biopharma’s Durham site to deliver quality drug substance at scale.

Lead the global cybersecurity program for a CDMO to protect intellectual property, regulated manufacturing systems, and client data while driving strategy, compliance, and incident response.

Eurofins is hiring an Onsite Upstream Biochemist in Indianapolis to run cell culture and bioreactor operations while supporting lab workflows and documentation.

IDBS seeks an experienced Account Manager to drive enterprise SaaS sales and expand strategic biopharma and biotech accounts across the US Northeast and Canada.

Join Editas Medicine as an mRNA Scientist I to execute IVT production, purification, and analytics in support of advancing CRISPR-based in vivo LNP programs toward clinical development.

Rentschler Biopharma is hiring a Senior MSAT Engineer (Downstream) in Milford, MA to lead downstream process transfers and ensure robust, GMP-compliant manufacturing execution for clinical and commercial biologics.

Catalent seeks an Accounting Analyst to support financial reporting, reconciliations, and process improvements at its St. Petersburg manufacturing site.

Lead commercial growth for SGS Health Science's biologics and biosafety services across New England by identifying, developing, and closing CDMO/CRO opportunities.

Lead a team of molecular and cellular biologists at Catalent’s Kansas City Biologics Analytical Services site, providing technical direction, GMP-compliant method development, and people management to support biologics product development.

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

Support upstream bioprocess operations at Eurofins Indianapolis by running flask cultures, operating WAVE and single-use bioreactors, sampling and harvesting, and maintaining accurate documentation and lab inventory.

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.

Experienced business development leader needed to grow Catalent's inhalation (nasal and pulmonary) services by generating new accounts, negotiating complex agreements, and driving cross-selling opportunities.

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.

Cellares is hiring a Senior Director, IDMO Site Quality to lead QA and QC for its Bridgewater cGMP cell therapy manufacturing site, driving quality systems, regulatory compliance, and team development.

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.

Lead technical strategy and execution for cell line development and tech transfer, delivering robust CLD and upstream process transfers to pharmaceutical and biotech partners from Asimov’s Boston site.