Regulatory Affairs And Pharmacovigilance Specialist
Ferring Pharmaceuticals
UK
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Minimum of 3 years regulatory experience
Knowledge of uk regulatory environment
Post-brexit regulatory requirements knowledge
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Ferring Pharmaceuticals is seeking a Regulatory Affairs and Pharmacovigilance Specialist in the UK, requiring a minimum of three years of experience in regulatory roles within the pharmaceutical industry. The position offers a hybrid work model and emphasizes an entrepreneurial culture focused on collaboration and innovation to improve health outcomes.
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Job Summary
The role involves preparing, reviewing, and submitting variations, renewals, and new product authorizations for the UK market.
Candidates must maintain the local UK Pharmacovigilance System Master File and monitor regulatory changes for the UK and Ireland.
Ferring offers an inclusive support package called 'Building Families at Ferring' providing equal policies for all employees.
Matching Summary
Match Score: 75
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Ferring Pharmaceuticals is seeking a Regulatory Affairs and Pharmacovigilance Specialist in the UK, requiring a minimum of three years of experience in regulatory roles within the pharmaceutical industry. The position offers a hybrid work model and emphasizes an entrepreneurial culture focused on collaboration and innovation to improve health outcomes.
**
Skills & Requirements
Must-have
Minimum of 3 years Regulatory experience
Knowledge of UK Regulatory environment
Post-Brexit regulatory requirements knowledge
Nice-to-have
Experience with UK Health Authority MHRA
Direct work experience in Pharmacovigilance
Entrepreneurial spirit and innovative mindset
Key Requirements
Life Science degree or equivalent
Minimum 3 years pharmaceutical regulatory experience
Mandatory knowledge of UK post-Brexit requirements
Work Rights
Must live within reasonable commutable distance to office