Job Description
Our client is a well-established, GMP-accredited pharmaceutical manufacturer based in Lancashire, known for producing high-quality pharmaceutical products for both UK and international markets.
Are you a skilled QC Analyst with a passion for pharmaceutical quality and compliance? Do you thrive in a GMP-regulated environment and enjoy working with cutting-edge analytical techniques? If so, we want to hear from you!
QC Analyst
Lancashire - commutable from Southport, Wigan, Preston, Blackburn, Clitheroe, Bury, Darwen.
Up to £35,000 per annum
As a QC Analyst, you will play a key role in ensuring the safety, efficacy, and compliance of pharmaceutical products through rigorous analytical testing.
The responsibilities of the QC Analyst include:
•\tConduct routine and non-routine testing of raw materials and finished pharmaceutical products.
•\tOperate and maintain analytical instruments including HPLC, GC, UV, and IR.
•\tPerform equipment calibration and ensure accurate documentation.
•\tInvestigate and document Out of Specification (OOS) and Out of Trend (OOT) results.
•\tSupport method development and validation activities.
•\tEnsure strict adherence to cGMP and internal quality standards.
•\tCompile, interpret, and report analytical data for R&D and regulatory purposes.
The ideal candidate for the QC Analyst post will have:
•\tBSc (or higher) in Chemistry, Pharmaceutical Sciences, or a related discipline.
•\t1–3 years of experience in a GMP-regulated pharmaceutical laboratory.
•\tProficient in HPLC; experience with GC, UV, and IR is advantageous.
•\tStrong attention to detail and ability to work independently.
•\tFamiliarity with regulatory guidelines (MHRA, FDA, ICH) is a plus.
In return, you’ll join a supportive team with opportunities for professional development, ongoing training, and career progression within a growing pharmaceutical business.