Compliance Jobs
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Director Regulatory Affairs
Director of Regulatory AffairsHybrid - San Mateo, CA Salary: $190,000-$210,000 (negotiable for the right candidate)Summary:A global biopharmaceutical company specializing in photomedicine, rare metabolic disorders, and peptide‑based therapeutics is seeking a tenacious Director of Regulatory Affairs to lead U.S. and global regulatory strategy across...
Director of Global Regulatory Affairs Strategy
EPM Scientific are partnering with a global biopharmaceutical company, specializing in photomedicine, rare metabolic disorders, and peptide‑based therapeutics. They are seeking a tenacious Director of Global Regulatory Affairs to lead U.S. and global regulatory strategy across a pipeline spanning preclinical through commercial programs. The company...
Sr QA Investigator
Sr Quality Assurance InvestigatorLocation: Lenoir, NCEmployment Type: Full-Time, On-SiteSalary Range: $65,000-$85,000/year Position SummaryA growing pharmaceutical manufacturing organization is seeking a Quality Assurance Investigator II to support its quality systems and compliance efforts. This role is responsible for investigating quality events...
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Process engineer
Location: Denmark (On-site) Contract Length: 6-12 monthsWe are supporting a client in Denmark with the hire of a Process Engineer to join the team on an initial 6-12 month contract.This position has opened due to increased project workload, and the successful candidate will provide hands-on process engineering support, with a strong focus on revie...
Director, CMC Quality Assurance
Director, CMC Quality AssuranceAre you ready to take your career to the next level in the heart of New York, United States? Our client, a prominent player in the biotech sector, is seeking a dynamic and experienced Director, CMC Quality Assurance. This exciting opportunity allows you to join an innovative environment, where you will play a critical...
QA
The role supports quality oversight of external manufacturers (CMOs) producing clinical trial products, within a highly matrixed, global environment. The position is non‑signature and does not include decision‑making authority. Job Title: QA / Clinical Quality Support ContractorContract: 1.5 years | Full‑time (40 hours/week) | Immediate start Key R...