Global Head

Company: Krug Associates
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Global Head of Manufacturing Science and Technology

Our client is a prominent international pharmaceutical company based in the UK seeking to appoint a Global Head of Manufacturing Science and Technology (MS&T). The role focuses on maintaining technical excellence and operational preparedness across the company’s external manufacturing partners.

Key Responsibilities

  • Manage projects and deliver scientific guidance in line with the overall business objectives.
  • Act as the primary subject matter expert supporting all MS&T initiatives.
  • Offer recommendations to project teams to secure timely delivery and adherence to necessary scientific standards.
  • Develop, maintain, and revise manufacturing process SOPs and related policies.
  • Prepare and keep current detailed manufacturing process maps.
  • Establish and implement advanced technology transfer frameworks and procedures, ensuring supporting documentation remains complete and up to date.
  • Champion continuous improvement and process optimisation initiatives that increase yield, lower costs, and enhance product quality throughout the manufacturing lifecycle.
  • Introduce and apply best‑in‑class project management tools across all initiatives, with regular reviews to maintain high standards.
  • Monitor external developments and keep teams informed of significant technical and strategic changes that may influence manufacturing approaches.
  • Lead and develop a team of technical and scientific specialists in the pharmaceutical field.

Education / Experience

  • BSc and MSc / PhD in Chemistry, Biochemical Engineering, or related field.
  • More than 10 years’ experience in pharmaceutical or biotech manufacturing, with strong expertise in process development—ideally covering both small and large molecules.
  • Demonstrated expertise in sterile manufacturing, fill‑finish processes, and packaging operations.
  • Solid knowledge of GMP and technical manufacturing, particularly in technology transfer.
  • Thorough understanding of CMC requirements and regulatory submissions to agencies such as EMA and FDA.
  • Inspiring leadership style combined with a practical, hands‑on approach to overseeing technical operations, complex projects, and cross‑functional teams.
  • Outstanding analytical, scientific, and communication abilities, with skill in explaining complex ideas to varied audiences.
  • Fluency in English.
  • Willingness to undertake international travel as needed.

Employment Details

Seniority level: DirectorEmployment type: Full‑timeJob function: Manufacturing, Management, and Project ManagementIndustry: Pharmaceutical Manufacturing

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Posted: June 4th, 2026