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Regulatory Affairs Specialist
2 months ago
Regulatory Affairs Specialist – Pharmaceuticals – Pharmaceutical Industry
A great opportunity has arisen with Science Solutions Recruitment Ltd, a leading pharmaceutical recruitment agency, to work as a Regulatory Affairs Specialist to progress your career within the pharmaceutical industry. This position is open to both regulatory professionals from either a pharmaceutical GMP background, or ideally a pharmaceutical GDP parallel import background.
Key responsibilities for the Regulatory Affairs Specialist position
- Ensure regulatory compliance with drugs imported overseas.
- Prepare initial application data forms & PLPI/PLGB initial applications.
- Lead any changes within regulations and ensure the quality management system (QMS) is compliant with these.
- Review and monitor licence applications to the Medicines and Healthcare products Regulatory Agency (MHRA).
- Manage supplier and vendor communication.
- Ensure all labelling is to MHRA regulations.
Requirements for the Regulatory Affairs Specialist position
- Hold a scientific degree.
- 2-3 years' experience within pharmaceutical regulatory (GMP or GDP).
- Expert organisational skills.
- Strong written and verbal communication skills.
- Innovative expertise.
Benefits for the Regulatory Affairs Specialist
- Free on-site parking.
- Flexibility on remote working.
- No weekends.
- 25 days' holiday & 8 bank holidays.
To be successful in this role, you will need to have a strong understanding of regulatory compliance and a proven track record of ensuring regulatory compliance within a pharmaceutical environment.
Science Solutions Recruitment Ltd is a leading pharmaceutical recruitment agency, and we are committed to finding the best talent for our clients. If you are a motivated and experienced regulatory professional looking to take your career to the next level, please apply for this exciting opportunity.