Regulatory Affairs and Compliance Manager
US$100,000 – US$120,000 / yr base salary
Posted 9 Oct 2026
Advertised as “Manager, Regulatory Affairs and Compliance”
BranchFactor Summary
The original posting with the fluff stripped out
- Expected experience
- 3–5 yrs
- Management level
- People management
- Employment
- On-Site
- Contract
- Full-time
| Base salary | US$100,000 – US$120,000 / yr |
|---|
Field of studyBiological Science, Chemical Science, Medical Laboratory Science, Physical Science
Study levelBachelor's
Study levelMaster's
Company Description
Eurofins Scientific is an international life sciences company, providing a unique range of analytical testing services to clients across multiple industries, to make life and our environment safer, healthier and more sustainable. From the food you eat, to the water you drink, to the medicines you rely on, Eurofins works with the biggest companies in the world to ensure the products they supply are safe, their ingredients are authentic and labelling is accurate.
Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as well as having an emerging global presence in Contract Development and Manufacturing Organisations. The Group also has a rapidly developing presence in highly specialised and molecular clinical diagnostic testing and in-vitro diagnostic products.
In over just 30 years, Eurofins has grown from one laboratory in Nantes, France to 55,000 staff across a decentralised and entrepreneurial network of 900 laboratories in over 50 countries. Eurofins offers a portfolio of over 200,000 analytical methods to evaluate the safety, identity, composition, authenticity, origin, traceability and purity of biological substances and products.
Job Description
GENERAL JOB DESCRIPTION
The Regulatory Affairs / Compliance Manager is responsible for ensuring that all laboratory processes, procedures, and outputs meet defined standards of quality and regulatory compliance. This role is critical in maintaining accreditation and delivering accurate and reliable testing results. The Manager designs and implements policies and procedures, conducts regular audits, manages documentation, and leads staff training initiatives to foster a culture of compliance and maintain the highest standards of quality and safety. This role coordinates cross-functional input.
KEY RESPONSIBILITIES
- Regulatory Oversight: Ensures alignment with relevant regulatory / accrediting bodies (e.g., FDA, CLIA, CAP, ISO, ASHI, etc.) Monitors effectiveness of the QMS through internal audits, indicators and reviews. Prevents fraud, abuse and negligence. Acts as primary point of contact and liaison for regulatory and accrediting bodies (e.g., FDA, CLIA, CAP, ISO, FDA). Coordinates and facilitates external inspections and audits. Promotes safe and lawful operations. Ensures inspection-readiness. Supports a culture of accountability and transparency.
- Governance and Reporting: Reports regulatory to executive leadership. Prepares compliance dashboards. Maintains audit information for investigations. Keeps up-to-date with FDA and State enforcement trends.