Job type
PermanentLocation
Greater LiverpoolWorking Pattern
Full-timeSpecialism
Quality Assurance And ValidationIndustry
Scientific and R&DPay
£35,000 - £40,000Closing date
3 Jun 2024
Regulatory | Quality | Full-Time | On-site | Cell Therapy
We are recruiting on behalf of a client who is looking to add a quality and regulatory affairs specialist to their growing team.
Regulatory Requirements
- Preparing submissions (GMP, MHRA, HTA).
- Engagement with regulatory bodies.
- Submitting licence approvals and maintaining these.
- Knowledge of UK, EMA, FDA regulations.
Qualifications
- Science or related degree.
- Extensive knowledge of regulations/guidelines.
Benefits
- 35 days holiday.
- House loan scheme.
- Flexible working.
- Enhanced maternity/paternity package.
- And more...