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Looking to uncover insights that could revolutionize the future of medicine and drive breakthroughs in patient care?

̽»¨ºÏ¼¯ is seeking an MSAT Associate Director to oversee the successful transfer and optimization of pharmaceutical manufacturing processes. In this role, you will leverage your scientific expertise to ensure compliance with GxP regulations, manage technical transfers between sites, and drive continuous improvement initiatives. You will work closely with internal teams and external partners to maintain product quality, resolve manufacturing challenges, and support portfolio growth. This position involves global collaboration and occasional travel to manufacturing sites.

Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.

Responsibilities:

• Ensure adherence to GxP regulations and standard operating procedures.
• Lead technical transfers of manufacturing processes, providing critical expertise and direction.
• Establish and track KPIs, budgets, and timelines for process transfers and improvements.
• Represent technical expertise in cross-functional projects, including supply chain, regulatory, and commercial activities.
• Provide scientific advice to procurement and regulatory teams, addressing batch failures, recalls, and variations.
• Conduct technical reviews and due diligence for potential acquisitions and divestments.
• Collaborate with manufacturing sites to optimize processes and resolve compliance or quality issues.
• Review and approve technical documentation, including certificates of analysis, stability data, and risk assessments.
• Manage quality records such as change control requests and deviations.
• Propose and implement technical and business improvements to enhance practices and systems.

Key Skills and Requirements:

• Degree in Life Sciences, Pharmacy, Pharmaceutical Sciences, or Chemistry.
• Proven experience in site-to-site technical transfers and pharmaceutical manufacturing processes.
• Familiarity with small molecule formats, including sterile products, capsules, creams, gels, ointments, and solid dose.
• Knowledge of Quality Management Systems, including change control and deviation management.
• Experience in operational budget management and strategic alignment.
• Proficiency in project management tools, templates, and methodologies.
• Strong problem-solving skills and ability to adapt to high-speed changes.
• Excellent organizational, communication, and time management skills.
• Demonstrated leadership and collaboration abilities across global teams.
• Commitment to continuous improvement and ethical standards.
  

If you are having difficulty in applying or if you have any questions, please contact Ed Little at e.little@proclinical.com.

If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.

̽»¨ºÏ¼¯ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ̽»¨ºÏ¼¯ is acting as an Employment Agency in relation to this vacancy.

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