QC Team Leader

JR United Kingdom; Wrexham; On-site; GBP 40,000 - 55,000; Full time

Job summary

A leading global pharmaceutical company is seeking an experienced QC Section Leader to manage analytical testing and ensure product quality. This role involves leading a team, ensuring compliance with regulations, and driving continuous improvement in QC processes. If you're ready for a new challenge in a rewarding environment, apply today!

Benefits

Competitive salary

Benefits

Qualifications

• Significant QC experience in a pharmaceutical environment.
• Experience managing a QC solid dose team.

Responsibilities

• Managing analytical testing of solid dose products.
• Leading a team to ensure product quality and compliance.
• Driving continuous improvement in QC processes.

Skills

Leadership

Quality Control

Analytical Skills

Education

BSc in Chemistry

BSc in Analytical Chemistry

Tools

HPLC

GC

UV

IR

Job description

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QC Section Leader

Location: North Wales – Site based, commutable from Deeside, Wrexham, Chester.

Salary: Competitive salary plus benefits

Are you an experienced QC Section Leader looking for the next step in your career? Are you seeking to develop your skills while working for an award-winning global pharmaceutical company? A rare opportunity has arisen to join one of the UK’s largest generic pharmaceutical companies as a QC Section Leader.

Reporting to the QC Manager, the responsibilities of the QC Section Leader include:

1. Managing the analytical testing of solid dose products using HPLC, GC, UV, and IR.
2. Leading a team of analysts to ensure product releases meet the highest standards of quality and consistency.
3. Ensuring all testing complies with cGMP, ALCOA+, Health and Safety, and COSHH regulations.
4. Critically reviewing analytical data and approving products for further processing when specifications are met.
5. Driving continuous improvement and ensuring compliance with industry regulations and company policies.

The ideal candidate will have:

1. A BSc in Chemistry, Analytical Chemistry, or a relevant scientific degree, with significant QC experience.
2. Experience managing the workload of a QC solid dose team, including preparing weekly and daily work schedules.
3. Experience leading OOS/OOT investigations and deviations.
4. Experience representing the QC group at internal, customer, and regulatory audits, and liaising with the regulatory affairs department.
5. Experience in analytical method transfer, verification, and validation is preferred.

If you are an experienced QC Section Leader seeking a new challenge, please apply today!