QC Section Leader

SRG; United Kingdom; On-site; GBP 42,000 - 50,000; Full time

Job summary

A leading pharmaceutical manufacturer in North Wales is seeking a QC Section Lead to manage a team and ensure compliance with GMP standards. You will oversee daily operations, lead investigations, and drive continuous improvement initiatives within the QC department. The ideal candidate has relevant qualifications and experience in a GMP environment. The position offers a competitive salary and various benefits including a pension scheme and subsidised canteen.

Benefits

Generous pension scheme

Annual holiday allowance

Subsidised on-site canteen

Social & sporting clubs

Free on-site parking

Qualifications

• Proven experience in a pharmaceutical laboratory or similar GMP environment.
• Previous experience of leading, supervising, or managing a team.
• Solid knowledge of pharmaceutical testing methods.

Responsibilities

• Managing the workload of the QC team, planning daily & weekly schedules.
• Motivating, mentoring & developing an effective QC team.
• Leading OOS/OOT investigations.
• Leading method transfer, verification & validation activities.
• Representing the QC group at internal & client meetings as well as audits.

Skills

Team management

GMP compliance

Problem-solving

Pharmaceutical testing methods

Education

Degree in Chemistry or similar qualification

Job description

QC Section Lead

42,000 - 50,000

North-Wales

SRG are recruiting for a QC Section Leader to manage a GMP QC team testing pharmaceutical products. Based in North Wales, this position will be based with a one of the UKs leading pharmaceutical manufacturers and will be responsible for ensuring the highest standards of quality are maintained and be a key figure in driving continuous improvement.

The Role:

Leading a team of analysts, you will manage day to day activities of the team and ensure key metrics and quality standards are maintained. Key responsibilities will include:

• Managing the workload of the QC team, planning daily & weekly schedules.
• Motivating, Mentoring & Developing an effective QC team.
• Leading OOS/OOT investigations.
• Leading method transfer, verification & validation activities
• Representing the QC group at internal & client meetings as well as audits.

Benefits:

• Generous pension scheme & annual holiday allowance
• Subsidised on-site canteen
• Social & sporting clubs
• Free on-site parking

Requirements:

• A degree or similar qualification in Chemistry or similar relevant qualification
• Proven experience in a pharmaceutical laboratory or similar GMP environment.
• Previous experience of leading, supervising or managing a team.
• Solid knowledge of pharmaceutical testing methods and experience of method transfer, verification & validation.

Carbon60, Lorien & SRG - The Impellam Group STEM Portfolio are acting as an Employment Business in relation to this vacancy.