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...
Regulatory Affairs Consultant
We are looking for an experienced Regulatory Affairs Consultant to support MDR transition, risk management, and validation documentation activities within a highly regulated pharmaceutical/medical device environment. This 12‑month hybrid assignment is based in Antwerp, working 2-3 days on‑site. Key ResponsibilitiesUpdate and rewrite Risk Management...
PAS-X Specialist Data Modelling Validation
A leading biopharmaceutical manufacturing site in Toulouse is seeking an experienced PAS‑X Validation Specialist to support ongoing MES/EBR deployment and data‑modelling activities. The specialist will work within the digital manufacturing and QA/CSV teams to ensure compliant design, configuration, and validation of PAS‑X workflows, MBRs, and syste...