Associate Director, Quality Assurance – Biopharma Manufacturing Location: Dundalk

Lead QA Excellence in Drug Product & Drug Substance GMP Operations Are you ready to shape the future of Quality Assurance in biopharmaceutical manufacturing? As Associate Director, QA, you’ll provide strategic oversight for Drug Product (DP) and Drug Substance (DS) GMP operations, ensuring compliance, driving continuous improvement, and leading a high-performing QA team. In this role, you will:

• Oversee GMP manufacturing and ensure compliance with regulatory standards.
• Lead QA support for tech transfers, PPQ, and inspection readiness.
• Build, mentor, and develop QA operations teams.
• Review and approve GMP documentation with a focus on data integrity.
• Champion continuous improvement initiatives to raise quality standards. What you bring:
• Degree in Biopharma or related scientific field.
• 8+ years’ experience in vaccine/biopharma DP/DS manufacturing (sterile filling a plus).
• Strong leadership, communication, and people management skills.
• A proven ability to collaborate across functions and solve complex challenges. Join us and make an impact by ensuring the highest standards of quality in delivering breakthrough therapies For further information on this Associate Director QA role in Dundalk please contact Caroline Kingston on +353 868395531 or email caroline@hero.ie Check out all our open jobs on our HERO Recruitment website – https://www.hero.ie/. Please Note: Under its obligation under the Data Protection legislation, HERO Recruitment will not forward your details to any company without your prior approval. Data can only be transferred outside of the EEA based on standards contractual clauses, to a country for whom an adequacy decision has been given by the European Commission or where the express permission of the data subject has been given. You have supplied us with your personal data in the process of applying for a position. Our client company may have personnel outside of the EEA who will review your data. We will apply the appropriate criteria in respect of the data transfer depending on the location of those personnel.