Quality Control Laboratory Analyst (GMP/GLP)

About the role

We are seeking a Quality Control Laboratory Analyst to join a large pharmaceutical company in Kent. The role involves performing analytical testing on raw materials, in‑process samples, finished products and composites to GMP/GLP standards.

Key responsibilities

• Conduct routine particle‑size analysis using Malvern Mastersizers and Sympatec instruments.
• Perform cleaning verification (HPLC) and identification testing (FTIR, Raman).
• Develop, validate and optimise analytical methods, including particle‑size and cleanability assessments.
• Run DSC, light microscopy, SEM, and Karl Fischer moisture analyses.
• Support technology transfer, pharmacopoeia analyses, CAPA investigations, deviation handling and document control.
• Work rotating shift patterns (early, late, night) over three‑week cycles.

Required profile

• Degree or equivalent in a scientific discipline.
• Experience in wet‑chemistry and analytical techniques within the pharmaceutical or related industry.
• Ability to work in clean‑room environments (clean‑shaven, no makeup, false eyelashes or nail varnish).

Required skills

• Particle‑size analysis (Malvern Mastersizer, Sympatec)
• HPLC
• FTIR and Raman spectroscopy
• Differential Scanning Calorimetry (DSC)
• Light microscopy
• Scanning Electron Microscopy (SEM)
• Karl Fischer moisture determination
• Method development and validation
• Technology transfer
• GMP/GLP compliance and document control
• CAPA handling

What we offer

• 12‑month contract with PAYE rate of £17.18 per hour (range £15‑£17.18).
• Potential for contract extension or permanent placement based on performance.
• Dynamic laboratory environment with exposure to a wide range of analytical techniques.