Regulatory Affairs Jobs at Ferring UK
Looking for impactful Regulatory Affairs Jobs that combine compliance, innovation, and patient-centric science? This Pharmacovigilance Specialist role offers a high-value jobs opportunity for life science graduates and experienced professionals seeking long-term growth. Located in the UK, this role stands out among Regulatory Affairs Jobs in the UK for its global exposure, hybrid flexibility, and meaningful contribution to patient safety and regulatory excellence.
About Ferring Pharmaceuticals
Ferring Pharmaceuticals is a research-driven, specialty biopharmaceutical company focused on reproductive medicine, women’s health, gastroenterology, and urology. With a strong global presence, Ferring offers some of the most respected Regulatory Affairs Jobs and Pharmacovigilance Specialist roles worldwide. The company’s people-first culture and long-term vision make it an excellent jobs opportunity for life science graduates and seasoned professionals alike.
Regulatory Affairs Job Details:
- Job Title: Regulatory Affairs and Pharmacovigilance Specialist
- Job Requisition ID: R0036190
- Location: West Drayton, United Kingdom
- Employment Type: Full Time
- Posted: Today
- Application Deadline: 1 March 2026 (30 days remaining)
- Work Model: Hybrid (minimum 3 days per week in the office)
About the Role
As a Regulatory Affairs and Pharmacovigilance Specialist, you will take responsibility for a broad range of activities across Regulatory Affairs, Compliance, Good Distribution Practice (GDP), and Good Pharmacovigilance Practices (GVP).
You will work closely with regulatory, quality, and safety colleagues, bringing an innovative, solutions-focused mindset, curiosity, and entrepreneurial spirit. Ferring will provide strong learning support to help you grow and succeed in this role.
Key Responsibilities
Regulatory Affairs
- Prepare, review, and submit variations, renewals, new product authorisations, and other regulatory filings, including packaging materials
- Monitor regulatory changes in the UK and Ireland, assess impact, and document updates in internal systems
- Manage and update data in the Regulatory Information Management System (RIMS)
- Handle requests for Certificates of Pharmaceutical Products (CPPs) and special statements
- Manage assessment and response processes for Parallel Trade Import Notifications (UK & Ireland)
Pharmacovigilance & Compliance
- Maintain and update the UK Pharmacovigilance System Master File (PSMF)
- Contribute to monthly Regulatory Affairs and Pharmacovigilance reports
- Act as Document Owner for assigned SOPs, policies, and regulatory/PV documentation
- Provide backup support for pharmacovigilance activities, including adverse event reporting and product quality complaints
- Ensure full compliance with GDP, GVP, and all applicable regulatory requirements
Qualifications & Experience
Required
- Life Sciences degree or equivalent
- Minimum 3 years’ regulatory experience within a pharmaceutical company (ideally 5 years)
- Strong knowledge of the UK regulatory environment, including post-Brexit requirements
Preferred
- Experience or working knowledge of the UK Pharmacovigilance environment
- Direct experience communicating with the MHRA
Benefits and Culture in Regulatory Affairs Jobs:
- “Building Families at Ferring” – inclusive global family-building policies
- Parental leave for both birthing and non-birthing parents
- Extended family-building support (subject to eligibility)
- A collaborative, respectful, and empowering work culture.
