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QC Chemistry Analyst - Pharmaceutical - Permanent - North West

Job Summary
As the QC Chemistry Analyst, you will be responsible for the design and carry 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

* A relevant science degree or equivalent qualification

* A sound understanding of current GMP, Health and Safety and COSHH regulations

* Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision

* The ability to take on a limited supervisory role would be an advantage

* 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