CareerAddict

Senior QC Analyst

CV-Library

Posted on Jun 19, 2026 by CV-Library
Pentre Maelor, Clwyd, United Kingdom
Pharmaceutical
Immediate Start
£26k - £33k Annual
Full-Time
Senior QC Analyst – Pharmaceutical Manufacturing | Wrexham

£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, HPLC, 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

Reference: 225270041

https://jobs.careeraddict.com/post/113435322
CV-Library

Senior QC Analyst

CV-Library

Posted on Jun 19, 2026 by CV-Library

Print
Pentre Maelor, Clwyd, United Kingdom
Pharmaceutical
Immediate Start
£26k - £33k Annual
Full-Time
Senior QC Analyst – Pharmaceutical Manufacturing | Wrexham

£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, HPLC, 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
Print

Reference: 225270041

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