Regulatory Affairs Manager (Medical Devices)
- Field: Medical & Pharmaceutical
- Deadline: 2026-03-13 11:03
- West London, London
Client Details
Our client is a cutting edge medical device manufacturer. They have multiple marketed products, as well as new products awaiting registration in UK, EU and ROW markets.
Description
Coordinate and manage regulatory submissions and approvals in line with industry standards.
Ensure compliance with applicable regulations and guidelines within the life sciences industry.
Monitor regulatory changes and update internal processes as required.
Provide strategic advice on regulatory matters to support business objectives.
Develop and maintain relationships with regulatory authorities and key stakeholders.
Prepare and review documentation to ensure accuracy and compliance.
Collaborate with internal teams to align regulatory strategies with organisational goals.
Support audits and inspections related to regulatory compliance.Profile
Proven record of working with Medical device regulations, and liaising with regulatory bodies.
Good knowledge of QMS activities.Job Offer
Competitive salary
4 Day Working week
Permanent position based in West London
