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