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Laboratory Analyst - Pharmaceutical QC & Stability Testing (2-Year FTC)
A well-established pharmaceutical company based in the Hertfordshire area is seeking a Laboratory Analyst to join their Analytical Development team on a 2-year fixed-term contract.
This is an ideal opportunity for someone with experience in quality control (QC) and analytical chemistry within a GMP-regulated environment to broaden their skills in a collaborative and high-quality lab setting.
Key Responsibilities - Analytical Chemistry & QC Testing
Perform quality control testing on raw materials, bulk products, and finished pharmaceuticals using HPLC, GC, and wet chemistry techniques.
Support stability testing for new product development and routine monitoring of commercial products.
Execute manual and automated assays in compliance with GMP standards.
Operate and maintain laboratory equipment and analytical instrumentation.
Record, analyse, and report data using Chromeleon, LIMS, Excel, and Word.
Contribute to the day-to-day operations of the lab, including equipment calibration and solvent disposal.
Candidate Requirements - Skills, Qualifications & Experience
Degree (or equivalent) in Chemistry or a related scientific discipline.
At least 1 year of experience in an analytical laboratory, ideally within a pharmaceutical GMP environment.
Hands-on experience with HPLC and GC techniques is essential.
Strong team player with effective verbal and written communication skills.
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