Head of Contract Performance

2 weeks ago


Cambridge, Cambridgeshire, United Kingdom Next Phase Recruitment Full time
Job Description

Next Phase Recruitment is seeking an experienced professional to fill the role of Head of Contract Performance in our client's state-of-the-art facility based near Cambridge. This position offers a unique opportunity to lead a growing manufacturing team and drive operational efficiency in the production of Advanced Therapy Medicinal Products (ATMPs).

Key Responsibilities
  • Develop and implement production strategies to meet client demands and business objectives, ensuring uninterrupted manufacture and supply of ATMPs.
  • Oversee the management of aseptic suites, using KPIs to identify areas for improvement and ensuring strict adherence to GMP and other regulations and internal quality standards.
  • Play a key role in facility design, capital projects, commissioning, and validation, with specific support for future cleanroom expansion.
  • Lead and manage a cross-functional team, providing guidance, training, and mentorship to ensure optimal performance and professional development throughout the department.
  • Provide strategic and scientific guidance in technical areas, supporting complex cell manufacturing, including technology transfer, maximising production efficiency, and implementation of new processes and automation.
  • Act as a production nominee/primary production point of contact during internal and external audits, including inspections by regulatory authorities.
  • Investigate, evaluate, and review existing practices and methodology, implementing improvements to ensure current quality standards are maintained, evaluated, and improved, as well as address any compliance-related concerns.
  • Perform tasks required for accreditation and licensing of the cleanroom facilities and clinical products by regulatory bodies, including the MHRA.
Requirements
  • BSc or MSc in a relevant scientific discipline (Pharmaceutical Sciences, Biotechnology, Biochemistry, or equivalent).
  • Significant experience and expertise in GMP manufacturing of ATMPs and significant experience in production management within the cellular therapy field, ideally in a CDMO setting.
  • Comprehensive understanding of cGMP, regulatory guidelines, and quality systems.
  • Experience of laboratory electronic management systems (LIMs, EMS, eBMR), project management, and planning.
  • Strong leadership and team management skills, with the ability to motivate and inspire others to foster a culture of collaboration, excellence, and continuous improvement.
  • Exceptional problem-solving and decision-making abilities, with a track record of meeting production targets and deadlines.

This is an exciting opportunity for a seasoned professional to take on a leadership role in a dynamic and growing company. If you are a motivated and experienced individual with a passion for ATMP production, we encourage you to apply for this position.



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