Bla Jobs

Lead Orchard’s US regulatory science strategy as Executive Director, advising cross-functional teams and managing FDA interactions to advance the company’s pipeline.

Senior scientific leader needed to define and execute preclinical strategy and oversee toxicology, DMPK, and bioanalytical programs supporting Scholar Rock’s biologics pipeline.

Allucent seeks a seasoned VP, CMC (contractor) to lead regulatory strategy, CMC development, and global Health Authority interactions to accelerate life-changing therapies.

Orchard Therapeutics seeks an experienced VP of Clinical Development to lead global clinical science, design and execute clinical strategies, and represent clinical development in regulatory and cross-functional engagements for its gene therapy programs.

Lead a Novartis Technical Operations program to deliver high-quality isotope products on time and drive strategic, compliant, and efficient site operations across the U.S.

Senior medical writer and team lead role responsible for authoring regulatory submissions and maturing medical writing processes at a growth-stage biotech focused on immunology.

Senior QA executive needed to lead Sirtex's global quality management system, drive FDA and international regulatory approvals for device and drug products, and manage a cross-functional QA organization from the Woburn hybrid office.

Lead enterprise CMC strategy and cross-functional teams at Bristol Myers Squibb to turn molecules into medicines across small molecules, biologics and new modalities.

Lead global regulatory strategy and submissions for Telix’s radiopharmaceutical portfolio, driving IND/BLA/MAA filings and agency interactions to support product approvals and international roll-out.

Pfizer is hiring a Principal Scientist in Bothell to lead formulation and physico‑chemical characterization for biotherapeutics, with an initial focus on ADCs and scale‑up to clinical and commercial manufacturing.

Lead analytical strategy and comparability for cell and gene therapies at Bristol Myers Squibb, driving cross-functional alignment, regulatory submissions, and technical governance.

Lead an analytical development team at AbbVie to design and implement robust separation-based methods and regulatory-ready analytical strategies supporting biologics development and GMP testing.

AbbVie's Pharma Principal Scientist will lead structural and physicochemical characterization of late-stage and commercial neurotoxin biologics to support regulatory submissions and lifecycle management.

Lead toxicology strategy and preclinical safety evaluation for high-impact global health R&D, guiding investments, due diligence, and cross-functional translation to advance safe, scalable interventions.

Gilead is hiring a Senior Manager, Project Management to lead Clinical Pharmacology project teams and drive submission-ready deliverables for lifecycle programs and regulatory filings.