Vacancy Detail
QC Pharmaceutical Laboratory Analyst
Talent STEM are currently looking to appoint the above role for a Biopharmaceutical client of ours.
What you’ll be doing
Perform routine and non-routine analytical testing on raw materials, in-process samples, finished product and stability samples, under established SOPs and regulatory standards (GMP / GLP / relevant quality frameworks).
Operate, maintain, calibrate and troubleshoot laboratory instrumentation (e.g. HPLC / UPLC, titrators, pH meters, UV/Vis, balances; plus additional equipment as required).
Prepare reagents, standards and samples; ensure accurate documentation of all test data in real time; maintain good data-integrity and compliance with quality standards.
Review analytical results, flag and investigate any out-of-specification (OOS) or out-of-trend (OOT) findings; escalate or support root-cause investigations and corrective actions, working with Quality Assurance or relevant teams.
Support method validation, method transfers, stability and release testing programmes as required; contribute to continuous improvement, SOP reviews and lab documentation updates.
Maintain a clean, audit-ready laboratory environment; manage inventory of reagents, consumables, glassware and equipment maintenance/qualification schedules.
Who we’re looking for
Degree (BSc or higher) in Chemistry, Biochemistry, Pharmaceutical Sciences, or a related scientific discipline — or equivalent lab experience.
Some prior lab experience, ideally within a QC / GMP-regulated environment. Entry-level candidates with strong lab training may be considered.
Familiarity with analytical techniques (HPLC/UPLC, titration, dissolution, UV/Vis, wet chemistry) and good working knowledge of lab instrumentation and data recording practices.
Attention to detail, good organisational skills, ability to work methodically under pressure and meet testing lead-time targets.
Good communication skills — able to liaise across QA, production, and technical teams; capable of contributing to investigations and documentation.
Flexibility, and willingness to adapt as the role evolves (method validation, stability work, cross-functional collaboration, etc.).
Why this opportunity stands out
Get in on the ground floor — we are building the QC / lab function ahead of a planned ramp-up, so early joiners have a real chance to shape lab processes and make their mark.
Work in a high-quality, regulated environment that values precision, compliance, and continuous improvement.
Opportunity to gain or expand experience with a broad range of techniques and contribute to both routine QC and developmental lab activities.
Dynamic environment with potential for growth, learning, and increasing responsibility.
Next steps
If you’re interested — send a brief CV / profile summary using this link to apply.
Location: Stevenage | Salary: | Job type: Contract | Posted: 03/12/2025
