Regulatory Affairs & Pharmacovigilance Specialist (UK)

Ferring Pharmaceuticals; West Drayton; Hybrid; GBP 60,000 - 80,000; Full time

Job summary

A global pharmaceutical company in West Drayton is seeking a Regulatory Affairs professional to manage various regulatory tasks, including filings and compliance monitoring. The ideal candidate will have a Life Science degree and a minimum of 3 years of regulatory experience, ideally in the UK environment. You will contribute to the company's mission of supporting diverse family journeys and will work in a hybrid model, expected to be in the office a minimum of 3 days a week.

Benefits

Parental leave for all parents

Extended support on family building journey

Inclusive support package for family policies

Qualifications

• Minimum of 3 years Regulatory experience in a pharmaceutical company.
• Knowledge of post-Brexit requirements in the UK.
• Experience in the UK Pharmacovigilance environment is preferable.

Responsibilities

• Prepare and submit regulatory filings and updates.
• Maintain the local UK Pharmacovigilance System Master File.
• Monitor regulatory changes for the UK and Ireland.

Skills

Regulatory experience

Knowledge of the UK Regulatory environment

Communication with the UK Health Authority

Pharmacovigilance knowledge

Curiosity and entrepreneurial spirit

Education

Life Science degree or equivalent

Job description

A global pharmaceutical company in West Drayton is seeking a Regulatory Affairs professional to manage various regulatory tasks, including filings and compliance monitoring. The ideal candidate will have a Life Science degree and a minimum of 3 years of regulatory experience, ideally in the UK environment. You will contribute to the company's mission of supporting diverse family journeys and will work in a hybrid model, expected to be in the office a minimum of 3 days a week.