Quality Control Laboratory Analyst GMP / GLP – Kent
Opportunity:
Are you currently working in analytical quality control? Does your experience include hands-on analytical testing of Raw Materials, In-process, Release, and Stability checks of drug products? Want to work for a large pharmaceutical company? If 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 are 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 troubleshooting, technology transfer, and pharmacopoeia analyses.
You will also be involved in CAPAs, deviations, and document control.
Working Hours:
* Early shift 6am - 2pm Monday-Friday – for 3 weeks then it changes to
* Late shift 1.30pm - 10pm Monday-Thursday, 1.30pm - 7pm Friday for 3 weeks then it changes to
* Night shift 9pm - 7am Monday - Thursday for 3 weeks then back to the early shift.
This is a 12-month contract based in Kent, which will be reviewed for a possible extension depending on the candidate and business performance. The PAYE rate is £14.76 per hour.
Skills:
* Degree or equivalent in a scientific subject.
* Experience in wet chemistry / analytical techniques ideally within the pharmaceutical or related industry.
How to Apply:
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If this role interests you or a colleague, please contact us. If we successfully fill a permanent position from your recommendation, you will receive a £300 cheque. We also offer various incentive schemes for referring contractors/temp staff. Contact us for more information.
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