Back to searchSenior QC Analyst
Kenton Black - Science & Engineering
Posted a day ago, valid for a month
Wrexham, Wrexham LL13 8DW, Wales
£40,000 per annum
Full Time
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Sonic Summary
- The position is for a Senior QC Analyst based in North Wales, commutable from Deeside, Wrexham, and Chester.
- The role offers a competitive salary along with benefits and requires a minimum of three years of experience in Quality Control (QC).
- Candidates should possess a BSc in Chemistry, Analytical Chemistry, or a relevant scientific degree, along with experience in the pharmaceutical industry.
- Responsibilities include performing HPLC/UPLC/UV/GC analytical testing, method validation, and monitoring the quality of pharmaceutical products.
- This is a rare opportunity to join one of the UK's largest generic pharmaceutical companies, ideal for detail-oriented individuals seeking career advancement.
Permanent
North Wales Site based, commutable from Deeside, Wrexham, Chester.
Competitive salary plus benefits
Are 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 Senior QC Analyst to join one of the UKs largest generic pharmaceutical companies.
Reporting in to the QC Manager, the Senior 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 Senior 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 validation
If you are an experienced QC Analyst looking for a new challenge then please apply today!
