QC Chemistry Analyst - Pharmaceutical - Permanent - North West
Job Summary
As the QC Chemistry Analyst, you will be responsible for the design and carrying out of HPLC/UPLC/UV/GC analytical method validation and verification. You will support the department to monitor the quality of components, raw materials, products, and production processes by sampling, inspection, and analysis.
Qualifications and Skills
1. A relevant science degree or equivalent qualification.
2. A sound understanding of current GMP, Health and Safety, and COSHH regulations.
3. Experience in designing validation and/or verification protocols, running method validation and/or verification studies, and the ability to write validation reports with minimal supervision.
4. The ability to take on a limited supervisory role would be an advantage.
5. Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validation.
Benefits
33 days holiday inclusive of Bank Holidays.
Pension Contributions 7% employer / 7% employee.
#J-18808-Ljbffr