Regulatory Affairs And Pharmacovigilance Specialist
Ferring Pharmaceuticals
London, United Kingdom
Hybrid
Minimum 3 years regulatory experience
Knowledge of uk regulatory environment
Post-brexit regulatory requirements knowledge
The role involves preparing, reviewing, and submitting regulatory filings such as variations, renewals, and new product authorizations for the UK market
Job Summary
The role involves preparing, reviewing, and submitting regulatory filings such as variations, renewals, and new product authorizations for the UK market.
Candidates must maintain the local UK Pharmacovigilance System Master File and ensure full compliance with Good Distribution Practice and Good Pharmacovigilance Practices.
Ferring offers an inclusive support package called 'Building Families at Ferring' which provides equal policies for all employees wishing to start their family journey.
Matching Summary
The role involves preparing, reviewing, and submitting regulatory filings such as variations, renewals, and new product authorizations for the UK market.
Skills & Requirements
Must-have
Minimum 3 years Regulatory experience
Knowledge of UK Regulatory environment
Post-Brexit regulatory requirements knowledge
Nice-to-have
Experience communicating with MHRA
Direct Pharmacovigilance work experience
Entrepreneurial spirit and curiosity
Key Requirements
Life Science degree or equivalent
Minimum 3 years pharmaceutical Regulatory experience
Mandatory knowledge of UK post-Brexit regulations
Work Rights
Must live within reasonable commutable distance to office