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Associate director – quality assurance, drug substance

Brightwater Recruitment
Associate director
€80,000 - €120,000 a year
Posted: 18 September
Offer description

Associate Director – Quality Assurance, Drug Substance & Drug Product

About the Company

Join an innovative biopharmaceutical company at the forefront of vaccine development. This growing site is building a dynamic team, focused on operational excellence, compliance, and cutting-edge technology in a fast-paced, startup-like environment.

About the Position

We are seeking an experienced Quality Assurance professional to lead the QA Operations team, covering both Drug Substance (DS) and Drug Product (DP) manufacturing. This pivotal role will ensure GMP compliance across the site, guide a growing team of specialists, and support the site through technology transfer and GMP readiness activities. The ideal candidate thrives in complex environments, is used to startup or early-stage manufacturing operations, and can combine hands-on expertise with strong leadership.

Key Responsibilities

* Act as the QA Operations lead for onsite quality monitoring of DS and DP manufacturing.
* Support technology transfer, shake down batches, and site GMP readiness initiatives.
* Lead and develop a QA Operations team (currently 4–6 FTEs), fostering accountability and strong performance.
* Review, approve, and audit manufacturing documentation to ensure regulatory and company compliance.
* Provide QA guidance across manufacturing and cross-functional teams, supporting compliance and continuous improvement initiatives.
* Support inspections and self-audits, providing coaching and guidance to the team.

Experience/Requirements

* Degree in Biopharmaceutical Science or a related discipline.
* Minimum 8 years' experience in vaccine or biopharma DS/DP manufacturing, with sterile filling experience highly desirable.
* Proven track record in managing a team, mentoring specialists, and driving operational excellence.
* Experience in startup or early-stage facility environments, including GMP readiness and inspections.
* Strong knowledge of European regulations, cGMP, and quality compliance standards.
* Excellent interpersonal and communication skills, able to work collaboratively in a matrix environment.
* Ability to adapt in a fast-changing environment, balancing compliance with operational demands.

Remuneration Package

* Competitive salary: up to €110k (with potential sign-on bonus)
* Annual bonus: 12% of salary (company and personal performance-based)
* Long-Term Incentives (performance-based, awarded over 3 years)
* DB and DC pension schemes
* 25 days' annual leave
* Full-time onsite role (with potential for future hybrid flexibility)

Contact Melissa Caramante on for full details.

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