CY Partners are currently looking to recruit a number of QC Analyst on behalf of a North East based Pharmaceutical CDMO.

This is a fantastic opportunity to join a growing industry and work on a diverse range of pharmaceutical products in a cGMP lab environment.

Requirements

• To perform analysis and report results in accordance with cGMP requirements for laboratory operations.
• To investigate analytical deviations and out of specification results with appropriate rigour and to contribute to their root cause resolution.
• To organise calibration and maintenance of analytical equipment.
• As required, to perform routine auditing of laboratory areas.
• To perform technical transfers between internal and external customers.
• To support cGMP stability programs.
• To characterise reference materials for use in cGMP analysis.
• Develop, evaluate and prepare analytical methods and SOPs as required.

• Ensure cGMP/GLP compliance

Requirements

• A minimum BSc in Chemistry or Pharmaceutical Science (or related) MSc desirable
• Prior experience in a cGMP Lab environment
• Experience using HPLC and GC as well as other Analytical and Wet Chemistry techniques
• Strong work ethic, attention to detail and communication skills.

Some roles will be permanent and some will start as initial 12 month contracts, leading to a permanent offer upon a successful temporary period.

If you are interested in this role, please contact Graham at CY Partners.

Tagged as: Analytical Chemistry, cGMP, GC, HPLC, Pharmaceutical