QC Validation Officer

Walker Cole International is currently searching for a QC Validation Officer to join a leading Liquid Pharmaceutical Manufacturer based in the North of England.

This is a unique opportunity to take on an R&D-focused role within a dynamic QC environment, where your work will directly impact products currently on the market.

Your responsibilities as QC Validation Officer would be to:

• Lead analytical method validation and support method development for liquid pharmaceutical products.
• Write and review protocols and reports to GMP standards.
• Oversee the work of two QC Analysts (without direct line management responsibility), offering guidance and coaching.
• Act as the main point of contact for ongoing QC validation projects, collaborating cross-functionally with R&D, QA and production teams.
• Play a central role in quality decision-making processes within a hands-on, fast-paced department.

We are searching for a candidate who:

• Holds a degree in a relevant scientific discipline (e.g., Chemistry, Pharmaceutical Sciences).
• Has strong experience in method validation and method development within a GMP-regulated environment.
• Is confident writing technical documentation including protocols and validation reports.
• Has hands-on experience using analytical techniques such as HPLC and GC.
• Is personable, proactive and able to coach others effectively.

This role offers a broader quality perspective and visibility across the full pharmaceutical lifecycle. It’s ideal for someone with an R&D background who wants to expand into more quality-focused work in a collaborative environment. With opportunities to grow and move laterally across functions, this is a great step for long-term career progression.

HPLC | Validation | Method Development | GMP | QC | Pharmaceuticals | Analytical Method Validation | Good Manufacturing Practice