Site Director - Quality Assurance (QA)

JR United Kingdom; United Kingdom; On-site; GBP 60,000 - 100,000; Full time

Job summary

An established industry player in the biopharmaceutical sector is on the lookout for a Site Director in Quality Assurance. This pivotal role involves managing the Site Quality team, ensuring compliance with stringent cGMP standards, and collaborating with senior stakeholders to uphold the highest quality standards for biopharmaceutical products. The successful candidate will lead continuous improvement initiatives and serve as the key Quality contact for external clients. If you have extensive experience in the GMP sector and a passion for quality, this opportunity is perfect for you.

Benefits

Relocation assistance

Professional development opportunities

Health insurance

Flexible working hours

Qualifications

• Extensive experience in GMP Biopharmaceutical or Pharmaceutical sectors.
• Proven leadership in supervisory roles within Quality Assurance.

Responsibilities

• Manage the Site Quality team ensuring compliance with cGMP standards.
• Oversee Technical Operations including QC and production.

Skills

Quality Assurance

GMP Compliance

Leadership

Root Cause Analysis

CAPA Management

Job description

Site Director - Quality Assurance (QA) - United Kingdom

Client:

Walker Cole International

Location:

South-West, UK

Job Category:

Other

EU work permit required:

Yes

Job Views:

3

Posted:

24.04.2025

Expiry Date:

08.06.2025

Job Description:

Relocation assistance on offer

Walker Cole International is seeking a Site Director - Quality Assurance (QA) to join a global biopharmaceutical company based in the South-West of the UK. The successful candidate will ensure the release of biopharmaceutical products meets the highest standards and regulatory requirements.

Responsibilities:

1. Manage the Site Quality team.
2. Ensure all activities comply with cGMP standards.
3. Collaborate with internal teams and liaise with senior stakeholders.
4. Serve as the Quality contact for external clients.
5. Oversee Technical Operations, including QC, production, and Engineering.
6. Support audits and regulatory inspections.
7. Contribute to continuous improvement initiatives related to quality objectives.

Qualifications and Experience:

• Extensive experience in GMP Biopharmaceutical, GMP Pharmaceutical, or medical devices sectors.
• Proven leadership in supervisory roles.
• Technical knowledge of cGMP guidelines, deviation & CAPA management, and audit processes.

Keywords: Quality Assurance, QA, Compliance, Operations, Site Quality Director, GMP, Biopharmaceutical, Pharmaceutical, Medical Devices, CAPA, Deviations, Root Cause Analysis, Out of Specification (OOS), Out of Trend (OOT).