Regulatory Affairs Manager

Senior International Consultant - Regulatory Affairs and Executive search

Senior Regulatory Affairs Manager – Europe

Slough – Hybrid. Full time, Permanent

This position supports and coordinates regulatory activities for both specialty and generic pharmaceutical products across Europe. The role involves strategic input into development programs, preparation and submission of regulatory documentation, and post-approval lifecycle management. You will work cross-functionally with internal teams and external partners to ensure timely and compliant submissions to EMA and national authorities.

• Lead regulatory strategy development for new and existing products, including De-centralised/orphan and generic submissions.
• Review non-clinical and clinical data packages for regulatory adequacy and compliance.
• Conduct due diligence across CTD Modules 1–5 and review sections of Marketing Authorisation Applications (MAAs).
• Coordinate registration and maintenance of assigned generic products.
• Support regulatory authority interactions, including scientific advice procedures.
• Maintain regulatory databases and document management systems.
• Guide junior staff and contribute to process improvements within the regulatory function.
• Ensure alignment with EU regulatory requirements for product launch and lifecycle activities.

• Strong, clear evidenced experience with European regulatory frameworks and submission pathways (DCP, MRP, national procedures).
• Proven experience in regulatory strategy development for specialty and generic products- minimum 7 years industry experience
• Hands-on experience with post-approval activities, variation strategies, line extensions and due diligence .
• Familiarity with regulatory tools and platforms (eCTD, CESP, MHRA portal, Eudralink).
• Ability to critically evaluate scientific data and identify regulatory risks and mitigation strategies.
• Degree or higher qualification in Pharmacy, Life Sciences, or a related field.
• Excellent communication, project management, and cross-functional collaboration skills.
• Experience managing regulatory timelines and approvals in a fast-paced environment.

All applicants must hold valid right to work as sponsorship is unavailable.

Must be located within a commutable distance to SL1 and comfortable working from the office at least 3 times per week.

• Mid-Senior level

• Full-time

• Consulting, Quality Assurance, and Other

• Pharmaceutical Manufacturing, Wholesale Drugs and Sundries, and Retail Pharmacies

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