QC Section Leader

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

Job summary

A leading pharmaceutical manufacturer in North Wales is looking for a QC Section Lead to oversee a GMP QC team responsible for testing pharmaceutical products. You will manage daily operations, mentor staff, and ensure quality standards are upheld. Candidates should have a degree in Chemistry and experience in a GMP environment. Benefits include a generous pension scheme, subsidized canteen, and free parking.

Benefits

Generous pension scheme

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 and experience of method transfer, verification & validation.

Responsibilities

• Manage the workload of the QC team, planning daily & weekly schedules.
• Motivate, mentor & develop an effective QC team.
• Lead OOS/OOT investigations.
• Lead method transfer, verification & validation activities.
• Represent the QC group at internal & client meetings as well as audits.

Skills

Leadership

Team Management

Pharmaceutical Testing Knowledge

Education

Degree in Chemistry or relevant 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.