Associate Director Quality Assurance

JR United Kingdom; London; Hybrid; GBP 70,000 - 100,000; Full time

Job summary

A leading biopharma organization in London is seeking an Associate Director of Quality Assurance to lead site-wide QA operations. This strategic role involves ensuring compliance with global regulatory standards, mentoring QA teams, and driving continuous improvement in a dynamic environment.

Benefits

Competitive salary with bonus potential

Flexible working hours, including some remote work

Opportunity to shape quality systems

Supportive, well-established team

Qualifications

• 10+ years of experience in Quality Assurance within GMP-regulated environments.
• Strong background in sterile manufacturing and quality system development.
• Deep understanding of global GxP standards.

Responsibilities

• Oversee development and governance of site-level Quality Systems.
• Lead and mentor cross-functional QA teams.
• Act as site lead during audits and regulatory inspections.

Skills

Leadership

Problem-solving

Communication

Education

Degree in life sciences or pharmacy

Advanced qualifications

Job description

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Associate Director Quality Assurance, London

Client:

Barrington James

Location:

London, United Kingdom

Job Category:

Other

EU work permit required: Yes

Job Views:

3

Posted:

23.05.2025

Expiry Date:

07.07.2025

Job Description:

An established and rapidly growing biopharma organization is seeking an Associate Director of Quality Assurance to lead the ongoing development, implementation, and compliance of site-wide Quality Assurance operations. This leadership role is critical in maintaining inspection readiness, overseeing Quality System processes, and fostering a culture of quality across cross-functional teams.

Key Responsibilities:

• Oversee the development and governance of site-level Quality Systems to ensure they meet global regulatory expectations.
• Lead and mentor cross-functional QA teams, including oversight of validation and supplier compliance functions.
• Act as site lead during audits and regulatory inspections, ensuring consistent state of readiness and timely follow-up on findings.
• Collaborate across departments to embed quality-focused practices into operations, training, and decision-making.
• Monitor evolving global GxP regulations and guide internal alignment to new standards.
• Drive continuous improvement through data-driven analysis and proactive risk mitigation.

Qualifications and Experience:

• 10+ years of experience in Quality Assurance within GMP-regulated pharmaceutical or biotech environments.
• Strong background in sterile manufacturing, validation, and quality system development.
• Deep understanding of global GxP standards, including EU, FDA, and ICH guidelines.
• Demonstrated ability to lead and scale QA teams in complex or high-growth environments.
• Excellent communication, leadership, and problem-solving skills.
• Degree in life sciences or pharmacy; advanced qualifications a plus.

Why Apply:

• Competitive salary with bonus potential
• Flexible working hours, including some remote work
• Strategic leadership role within an innovative biotech environment
• Opportunity to shape quality systems at a high-impact clinical site
• Occasional travel with primary focus on UK operations
• Supportive, well-established team with room for influence

If you are a highly motivated QA professional with leadership experience and a strong background in GMP compliance, we encourage you to apply.