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This job is no longer availableRegulatory Affairs Officer (Hybrid working)
I currently have a great opportunity for a Regulatory Affairs Officer to progress or start their career within Parallel import. This position is open for both Regulatory and Quality Assurance professionals, so please if you are unsure, give me a call .
Key responsibilities for the Regulatory Affairs Officer (Hybrid working)
- Ensure Regulatory compliance with drugs imported overseas.
- Lead any changes within the regulations and ensure the QMS is complaint with these.
- Review and monitor licence applications to the MHRA.
- Manage Supplier and Vendor communication.
- Ensure all labelling is to MHRA regulations.
Requirements for the Regulatory Affairs Officer (Hybrid working)
- Hold a Scientific Degree.
- 1 years’ experience within Pharmaceutical or Medical Device Regulatory Affairs or 5 + years within Quality Assurance
- Expert organisation skills
- Strong written and verbal communication skills.
Benefits for the Regulatory Affairs Officer (Hybrid working)
- Free on-site parking.
- Hybrid working policy up to 4 days remote
- No weekends.
- 25 Days holiday +Â bank holidays.
To apply for the Regulatory Affairs Officer (Hybrid working) or here more information, please contact Liam Shannon at Science Solutions Recruitment on .
