Quality Control Laboratory Analyst GMP​/GLP

Quality Control Laboratory Analyst GMP / GLP – Kent

Opportunity:
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!

Your role as a Quality Control Analytical Laboratory Analyst GMP/GLP based in Kent will involve testing raw materials, finished products, in process controls and composite samples to GMP / GLP standards.

Testing techniques may include, but is not limited to:

• Routine particle size analysis (Malvern Mastersizers, Sympatec)
• Cleaning verification (HPLC)
• Identification testing (FTIR and Raman)
• Method development and validation (including particle size and cleanability assessments)
• DSC
• Light microscopy
• SEM
• Moisture content (Karl Fisher)
• Method optimisation and trouble‑shooting
• Technology transfer and pharmacopoeia analyses

You will also get involved in CAPA's, deviations and document control.

Hours of work:

• Early shift 6am – 2pm Monday‑Friday for 3 weeks, then changes to
• Late shift 1.30pm – 10pm Monday‑Thursday, 1.30pm – 7pm Friday for 3 weeks, then changes to
• Night shift 9pm – 7am Monday‑Thursday for 3 weeks, then back to the early shift.

This is a 6‑month contract which will be reviewed for a possible extension or go permanent but this is all dependent on the candidate and business performance. The PAYE rate is £17.18 per hour.

• Degree or equivalent in a scientific subject.
• Experience in wet chemistry/analytical techniques ideally within the pharmaceutical or related industry.

To apply for this one‑off opportunity, please send a Word copy of your CV to me now by clicking on the Apply button or call me for a confidential chat. Please ensure you have read and agree to our Privacy Policy which can be found on the Quality Start website.