Build the Quality & Regulatory Teams That Protect Products & 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 organizations 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. The talent we place understands the science, knows the agencies, and can drive products to market with confidence. Role expertise spans Regulatory Affairs Associates, Regulatory Affairs Managers, Regulatory Affairs Directors, VPs of Regulatory Affairs, Global Regulatory Leads, and Regulatory Strategy Consultants.
Regulatory Operations
Regulatory operations professionals ensure submissions are assembled accurately, published to the right standards, and tracked across complex global dossiers. The detail-oriented, process-driven professionals this function demands are exactly who we find, from Regulatory Operations Managers, Submissions Managers, Regulatory Project Managers, to Document Management Specialists, eCTD Publishing Specialists, and Regulatory Operations Directors.
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. The specialists we recruit navigate this intersection of science, manufacturing, and regulation with authority, spanning Regulatory CMC Specialists, CMC Managers, CMC Directors, CMC Regulatory Leads, Drug Substance/Drug Product Specialists, and VPs of CMC Regulatory Affairs.
Quality
From the systems that underpin compliance to the release decisions that put products in patients' hands, quality professionals span two critical disciplines. The talent we place across quality assurance and quality control is technically rigorous, inspection-ready, and commercially aware enough to operate at pace in demanding environments. Roles covered include QA Associates, QA Managers, Quality Systems Managers, Compliance Managers, Qualified Persons (QP), Heads of Quality, VPs of Quality Assurance, QC Analysts, QC Scientists, QC Managers, Laboratory Managers, Microbiology Specialists, and QC Directors.
TESTIMONIALS
Looking to hire?
Get a tailored plan to source top quality & regulatory talent for your life sciences organisation today.
Looking for a new role?
Discover the latest quality & regulatory career opportunities or send us your CV and register today.