QC Supervisor

TieTalent; Wrexham; On-site; GBP 35,000 - 50,000; Full time

Job summary

A global manufacturing business near Wrexham is seeking a QC Supervisor to manage analytical testing and ensure compliance with industry standards. The ideal candidate has a chemistry degree and experience in a pharmaceutical environment. Responsibilities include leading a team of analysts and driving continuous improvement. This position offers a competitive salary and benefits.

Benefits

Competitive Salary

Benefits

Qualifications

• Experience in a pharmaceutical or similar laboratory environment.
• Understanding of GMP, Health and Safety, and COSHH regulations.
• Manage workload of the QC solid dose team, including scheduling.

Responsibilities

• Manage the analytical testing of solid dose products.
• Critically review analytical data and approve products for processing.
• Lead a team of analysts to ensure high standards of quality.

Skills

Supervisory skills

Interpersonal skills

Analytical skills

Education

Science degree in Chemistry or equivalent

Job description

About

QC Supervisor

Competitive Salary + Benefits

Wrexham, Days Only

gap technical are proud to be representing this global manufacturing business in their search for a QC Section Leader to work at their facility near Wrexham.

Performance Objectives

1. Manage the analytical testing of solid dose products.
2. Ensure all testing complies with cGMP, Health and Safety, and COSHH regulations.
3. Critically review analytical data and approve products for further processing when specifications are met.
4. Lead a team of analysts to ensure product release meets high standards of quality and consistency.
5. Drive continuous improvement and ensure compliance with industry regulations and company policies.

Person Specification

• Science degree in Chemistry or equivalent qualification.
• Experience in a pharmaceutical or similar laboratory environment.
• Understanding of GMP, Health and Safety, and COSHH regulations.
• Supervisory and interpersonal skills.
• Manage workload of the QC solid dose team, including scheduling.
• Experience in leading OOS/OOT investigations and deviations.
• Experience representing QC at audits and liaising with regulatory affairs.
• Experience in analytical method transfer, verification, and validation is preferred.

Application Process

Please send your CV via the 'Apply now' option on the website. For questions or other opportunities, please contact us.

This vacancy is advertised on behalf of gap technical, operating as an employment agency. We are committed to selecting and developing the best people based on suitability for the job.

Additional Information

Closing Date: 24/08/2025

Location: Wrexham, Wales, United Kingdom

Languages: English