Associate Director Quality Assurance

Social network you want to login/join with: Associate Director Quality Assurance, slough col-narrow-left Client: Barrington James Location: slough, United Kingdom Job Category: Other – EU work permit required: Yes col-narrow-right Job Views: 2 Posted: 31.05.2025 Expiry Date: 15.07.2025 col-wide Job Description: An established and rapidly growing biopharma organization is seeking a Associate Director of Quality Assuranceto 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. #J-18808-Ljbffr