Quality Control Analyst

Cpl Life Sciences is collaborating with a global, research‑led pharmaceutical company focused on developing high‑quality medicines, with a strong emphasis on science, quality, and improving patient outcomes worldwide.

This role is responsible for ensuring all materials are tested in line with approved specifications, procedures, and timelines, supporting the timely release and distribution of pharmaceutical products in compliance with GMP and quality standards.

Key Responsibilities

• Perform QC testing of materials in line with approved specifications.
• Qualify, maintain, and calibrate laboratory equipment (URS, IQ, OQ, PQ).
• Maintain laboratory quality systems and documentation.
• Support audits, inspections, deviations, CAPAs, and change controls.
• Support stability programmes, tech transfer activities, and data reporting (e.g. PQRs, KPIs).
• Collaborate cross‑functionally with Quality, Manufacturing, Supply Chain, and Regulatory teams.

Skills & Experience

• Strong knowledge of QC, GMP, and pharmaceutical manufacturing/packaging.
• Ability to interpret data and apply sound scientific judgement.
• Comfortable working cross‑functionally in a regulated environment.
• Good communication, organisation, and time‑management skills.

For more information, please contact me at lucy.kirkaldy@cpl.com

This role does NOT offer job sponsorship, and you must be close to the site and be able to work 100% on site.