QC Section Leader in Wrexham

Gap Technical Ltd; Wrexham; On-site; GBP 30,000 - 45,000; Full time

Job summary

A leading global manufacturing business is seeking a QC Section Leader for their Wrexham facility. The role focuses on managing quality control testing and compliance with regulatory standards, driving continuous improvement within the QC team. Candidates should possess a Science degree in Chemistry and relevant experience in a pharmaceutical environment.

Qualifications

• Science degree in Chemistry or equivalent qualification.
• Previous experience in a pharmaceutical lab environment is essential.
• Understanding of GMP, Health and Safety, and COSHH regulations.

Responsibilities

• Manage the analytical testing of solid dose products.
• Lead the QC team ensuring product quality and consistency.
• Oversee compliance with industry regulations and internal policies.

Skills

Analytical Skills

Team Leadership

Regulatory Compliance

Education

Science degree in Chemistry

Job description

QC Section Leader
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 based near Wrexham
Performance Objectives

• To manage the analytical testing of solid dose products.
• To ensure that all testing is carried out within the requirements of cGMP, Health and Safety and COSHH.
• To critically review analytical data, and where specifications are met, approve products for further processing.
• In this role, you will be responsible for leading a team of analyst and ensuring that release of our product meet the highest standards of quality and consistency.
• You will be a key player in driving continuous improvement and ensuring compliance with industry regulation and company polices.

Person Specification

• Science degree in Chemistry or equivalent qualification.
• Previous experience within a pharmaceutical or equivalent laboratory environment is essential.
• A thorough understanding of current GMP, Health and Safety and COSHH regulation and sound supervisory and interpersonal skills.
• Manage the workload of the QC solid dose team, including preparing weekly and daily work schedules.
• Previous experience in leading OOS/OOT investigations and deviations is essential.
• Previous experience in leading a team is preferred.
• Previous experience in representing the QC group at internal, customer and regulatory audits and liaising with the regulatory affair department is essential
• Experience in leading the analytical method transfer, verification and validation is preferred

Apply
Please send your CV via the Apply now option on the website
If you have any questions or are interested in any other opportunities we may have, please do not hesitate to get in touch
This vacancy is being advertised on behalf of gap technical who are operating as an employment agency.
gap technical are committed to the selection, recruitment and development of the best people, basing judgements solely on suitability for the job.
Closing Date: 16/08/2025
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