Associate Director Quality Assurance

Barrington James
London
6 days ago
Applications closed

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An established and rapidly growing biopharma organization is seeking a 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.

Apply to be considered!

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