QC Chemist supporting analytical testing of samples in a cGMP-compliant environment for pharmaceutical ingredients. Ensuring product quality and compliance with ICH guidelines and internal procedures.
Responsibilities
Support analytical testing of in-process, raw material, and finished product samples in a cGMP-compliant environment
Perform in-process analysis for different products using variety of analytical techniques (e.g. HPLC, Karl Fisher (KF), Loss on Drying (LOD)) with minimum delay to the production
Organise and prioritise the samples received to minimise delay to production
Ensure effective communication with supervisors and manufacturing operators
Maintain the instruments in the laboratory
Ensure all investigations are escalated to the Supervisor
Assist in the preparation and/or review of Standard Operating Procedure (SOP)
Perform duties in a safe and efficient manner including good housekeeping of laboratory area
Requirements
Required Degree in Analytical Science or equivalent HND/HNC
2 years' experience in a Quality role, ideally in fine chemicals or Pharmaceuticals
Demonstrate expertise in chemical analysis, including chromatographic separation techniques (e.g. HPLC and GC)
Experience in working to cGMP and ICH guidelines
Experienced in performing duties in accordance with site EOHS requirements
Good teamwork skills
Ability to work to moving deadlines, flexible approach to people and situations
Benefits
25 days’ annual leave plus recognised Scottish public holidays
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