✨ Senior QC Analyst – Pharmaceutical Manufacturing | North Wales ✨
£26,000–£33,000 DOE | Monday–Friday, 8:15am–4:15pm
Are you a detail‑driven analytical scientist with a passion for quality? A brilliant opportunity has opened for a Senior QC Analyst to join one of the UK’s leading pharmaceutical manufacturers, supporting the production of high‑quality medicines.
What You’ll Be Doing
In this senior role, you’ll take ownership of analytical method validation and verification using HPLC, UPLC, UV and GC. You’ll support the QC function by monitoring the quality of raw materials, components, products and processes through inspection, sampling and analysis.
You’ll also design and execute validation/verification protocols and produce clear, accurate validation reports with minimal supervision.
What We’re Looking For in the Senior QC Analyst
You’ll thrive here if you bring:
- A relevant science degree (or equivalent)
- Strong understanding of GMP, Health & Safety, and COSHH
- Hands‑on experience designing and running method validation/verification studies
- Proven experience in a pharmaceutical or regulated laboratory environment
- The ability to take on some light supervisory responsibilities (advantageous)
If you’re an experienced QC Analyst with a solid GMP background and strong analytical understanding and validation experience, we’d love to hear from you.
PLEASE NOTE: Sponsorship is not available with this role.
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