QC AnalystPermanentNorth Wales – Site based, commutable from Deeside, Wrexham, Chester.Up to £30,000 per annum plus benefitsAre you an experienced QC Analyst looking for the next step in your career? Are you a quality driven individual with a keen eye for detail? I may have the perfect opportunity for you!A rare opportunity has arisen for a QC Analyst to join one of the UK’s largest generic pharmaceutical companies.Reporting in to the QC Manager, the QC Analyst will be expected to:• Perform HPLC/UPLC/UV/GC analytical testing on a range of pharmaceutical raw materials and finished products.• Perform analytical method validation and/or verification • Support the department to monitor the quality of components, raw materials, products and production processes by inspection, sampling and/or analysis.The successful candidate for the QC Analyst role will have: • A BSc in Chemistry or Analytical Chemistry or relevant scientific degree, with at least three years’ experience in QC. • Previous experience from within the Pharmaceutical industry • Experience of designing validation, and/or verification protocols, running method validation, and/or verification studies and be able to write validation reports with minimal supervision• Relevant experience in a pharmaceutical or equivalent laboratory environment and proven industry experience performing analytical validationIf you are an experienced QC Analyst looking for a new challenge then please apply today!
Back to searchQC Analyst
Kenton Black Science & Engineering
Posted a day ago, valid for 4 days
Wrexham, Wrexham LL13 9PS, Wales
£30,000 per annum
Full Time
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Sonic Summary
- The job is for a permanent QC Analyst position located in North Wales, with a salary of up to £30,000 per annum plus benefits.
- The role involves performing analytical testing on pharmaceutical raw materials and finished products, including HPLC/UPLC/UV/GC methods.
- Candidates must have a BSc in Chemistry or Analytical Chemistry and at least three years of experience in quality control within the pharmaceutical industry.
- Responsibilities include analytical method validation, monitoring quality through inspection and analysis, and writing validation reports with minimal supervision.
- This is a great opportunity for quality-driven individuals seeking to advance their careers in a leading UK generic pharmaceutical company.
