Regulatory Manager – UK, CH & International Markets
CV-LibraryLondonpermanentPosted: 17 June 2026
Apply NowRegulatory Manager – UK, CH & International Markets
Walker Cole International is supporting a growing speciality pharmaceutical company in the search for a Regulatory Manager to join its Regulatory Affairs team.
This is an excellent opportunity to join a dynamic, patient-focused organisation with a growing international portfolio. The successful candidate will support regulatory activities across the UK, Switzerland, and international markets, ensuring product compliance and driving lifecycle management activities.
Key Responsibilities
• Manage regulatory submissions including variations, renewals, and marketing authorisation activities
• Support product lifecycle management across UK, Switzerland, and ROW markets
• Review product information, labelling, and artwork updates
• Lead regulatory Change Controls and communicate regulatory changes to internal and external stakeholders
• Collaborate with Quality, Pharmacovigilance, Medical Affairs, and CMOs
• Support product acquisitions, due diligence activities, and portfolio integration projects
About You
• Experience in Pharmaceutical Regulatory Affairs
• Strong knowledge of lifecycle management, variations, and renewals
• Exposure to UK, CH, and international regulatory procedures
• Experience working cross-functionally in a fast-paced environment
• Proactive, organised, and solution-oriented mindset
Regulatory Affairs / Regulatory Manager / Lifecycle Management / Variations / Renewals / MHRA / Swissmedic / ROW / International Regulatory Affairs / Pharmaceutical Industry / Change Control / Artwork / Due Diligence / UK/(phone number removed)
Walker Cole International is supporting a growing speciality pharmaceutical company in the search for a Regulatory Manager to join its Regulatory Affairs team.
This is an excellent opportunity to join a dynamic, patient-focused organisation with a growing international portfolio. The successful candidate will support regulatory activities across the UK, Switzerland, and international markets, ensuring product compliance and driving lifecycle management activities.
Key Responsibilities
• Manage regulatory submissions including variations, renewals, and marketing authorisation activities
• Support product lifecycle management across UK, Switzerland, and ROW markets
• Review product information, labelling, and artwork updates
• Lead regulatory Change Controls and communicate regulatory changes to internal and external stakeholders
• Collaborate with Quality, Pharmacovigilance, Medical Affairs, and CMOs
• Support product acquisitions, due diligence activities, and portfolio integration projects
About You
• Experience in Pharmaceutical Regulatory Affairs
• Strong knowledge of lifecycle management, variations, and renewals
• Exposure to UK, CH, and international regulatory procedures
• Experience working cross-functionally in a fast-paced environment
• Proactive, organised, and solution-oriented mindset
Regulatory Affairs / Regulatory Manager / Lifecycle Management / Variations / Renewals / MHRA / Swissmedic / ROW / International Regulatory Affairs / Pharmaceutical Industry / Change Control / Artwork / Due Diligence / UK/(phone number removed)