Build the Quality & Regulatory Teams That Protect Products and Patients
In life sciences, quality and regulatory excellence is non-negotiable because one gap in your team can delay a submission, stall a launch, or put patients at risk.
EPM Scientific places the regulatory affairs, regulatory operations, regulatory CMC, quality assurance, and quality control professionals who keep organisations compliant, inspection-ready, and moving forward, across pharma, biotech, and medical devices.
Quality & regulatory talent solutions, bespoke to you
The right quality or regulatory hire protects your products, your submissions, and your patients. Here's how we help.
Hiring for your business
Quality and regulatory hiring demands a partner who understands GxP compliance, submission timelines, and the cost of getting it wrong.
Looking for a new role?
Browse the latest quality and regulatory roles across life sciences, with expert support from first conversation to final offer.
Adding value
Compensation benchmarking, talent mapping, and market intelligence to help you hire smarter and move forward with confidence.
Specialist quality & regulatory expertise
Quality and regulatory professionals must combine deep technical knowledge with the judgement to navigate evolving global frameworks. Finding that at the right seniority, therapeutic area, and geography is what we do.
Regulatory Affairs
Regulatory affairs professionals define the pathway, manage agency interactions, and ensure submissions are compelling, compliant, and on time. We place regulatory affairs talent who understand the science, know the agencies, and can drive products to market with confidence. Roles include: Regulatory Affairs Associate · Regulatory Affairs Manager · Regulatory Affairs Director · VP of Regulatory Affairs · Global Regulatory Lead · Regulatory Strategy Consultant
Regulatory Operations
Regulatory operations professionals ensure submissions are assembled accurately, published to the right standards, and tracked across complex global dossiers. We place the detail-oriented, process-driven professionals this function demands. Roles include: Regulatory Operations Manager · Submissions Manager · Regulatory Project Manager · Document Management Specialist · eCTD Publishing Specialist · Regulatory Operations Director
Regulatory CMC
CMC is one of the most technically demanding areas within regulatory affairs. Professionals must translate complex manufacturing science into clear, agency-ready documentation and defend it under scrutiny. We recruit specialists who navigate this intersection of science, manufacturing, and regulation with authority. Roles include: Regulatory CMC Specialist · CMC Manager · CMC Director · CMC Regulatory Lead · Drug Substance/Drug Product Specialist · VP of CMC Regulatory Affairs
Quality
From the systems and culture that underpin compliance to the testing and release decisions that put products in patients' hands, quality professionals span two critical disciplines. We place both quality assurance and quality control talent, professionals who are technically rigorous, inspection-ready, and commercially aware enough to operate at pace in demanding environments. Roles include: QA Associate · QA Manager · Quality Systems Manager · Compliance Manager · Qualified Person (QP) · Head of Quality · VP of Quality Assurance · QC Analyst · QC Scientist · QC Manager · Laboratory Manager · Microbiology Specialist · QC Director
TESTIMONIALS
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