QC Chemistry Analyst

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