Quality Control Laboratory Analyst GMP / GLP – Kent

Quality Control Laboratory Analyst GMP / GLP – Kent

Are you currently working in analytical quality control? Does your experience include hands on particle size analysis, analytical testing of Raw Materials, In-process, Release and Stability checks of drug products? Want to work for a large pharmaceutical company? Yes then this is the role for you!

Responsibilities

• Test raw materials, finished products, in‑process controls and composite samples to GMP/GLP standards.
• Perform routine particle size analysis (Malvern Mastersizers, Sympatec).
• Conduct cleaning verification (HPLC), identification testing (FTIR and Raman), method development and validation, DSC, light microscopy, SEM, moisture content (Karl Fisher).
• Optimize and troubleshoot analytical methods and participate in technology transfer and pharmacopoeia analyses.
• Involve in CAPA’s, deviations and document control.

Contract & Hours

12‑month contract with review for possible extension or permanent placement, dependent on performance. PAYE rate: £17.18 per hour.

• Early shift: 6 am – 2 pm, Monday‑Friday for 3 weeks before switching.
• Late shift: 1.30 pm – 10 pm, Monday‑Thursday; 1.30 pm – 7 pm, Friday for 3 weeks before switching.
• Night shift: 9 pm – 7 am, Monday‑Thursday for 3 weeks before returning to early shift.

Qualifications & Skills

• Degree or equivalent in a scientific subject.
• Experience in wet chemistry/analytical techniques, ideally within the pharmaceutical or related industry.
• Clean‑shaven; no makeup, false eyelashes, or nail varnish due to clean‑room requirements.

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