Exciting opportunity to begin or progress your career in Quality Assurance in a world leading laboratory in Manchester!
Joining a dynamic and friendly team, you will work meticulously to review analytical data to ensure there are no mistakes in study documentation. You will examine all reports and paperwork, including checking of technical calculations, and report any errors to the author. As a result of the wide variety of studies completed onsite, you will be responsible for reviewing a large range of analytical data for GMP, GLP & GCP regulated projects.
To be considered for this role, you must have:
* A minimum of 12 months industry experience, ideally working with HPLC and/or GC instrumentation
* Exemplary attention to detail
* Confidence to highlight errors to all seniority of staff
* Excellent communication & interpersonal skills
* A passion for quality assurance and data integrity
These roles are offered on a permanent or temporary basis.
If you’d like to develop your career in Quality Assurance in a successful and expanding laboratory, then apply to VRS today!
Key words: quality assurance, QA, data checking, data integrity, QC, quality control, study documentation, reports, analytical, HPLC, GC, pharmaceutical, biopharmaceutical, GMP, GCP, GLP, Manchester, VRS6130AW
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