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The Regulatory Affairs Manager will play a fundamental role in maintaining continued regulatory compliance with standards and medical device regulations. The ideal candidate will join a dynamic team launching innovative technology. 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 salary4 Day Working weekPermanent position based in West London