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.