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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Associate Director Regulatory Affairs
Associate Director / Director Regulatory AffairsConfidential Early‑Stage Biotech | San Diego, CA (Onsite Preferred / Hybrid Considered)Expected Compensation: $180-$200k base + bonus + equityWe're supporting a confidential, venture‑backed RNA therapeutics company in San Diego. They're backed by top-tier global biotech investors, and developing a pip...
Quality Manager IVD (London)
Quality Manager - PCR IVD Innovation,London. Fast‑Growing Diagnostics Scale‑UpJoin one of the most exciting diagnostic innovators as they expand their PCR testing platform globally. As Quality Manager, you'll be the driving force behind a world‑class quality system that supports breakthrough molecular diagnostics across the UK Healthcare market. Th...
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...