We are seeking an MSAT Manager to lead technology transfer activities into GMP manufacturing within an advanced biopharmaceutical manufacturing environment.
Reporting into the leadership team, this is a highly visible role responsible for bridging the gap between process development and GMP operations, ensuring manufacturing processes are successfully transferred, implemented, and executed within a regulated setting.
This role combines technical leadership, people management, and customer engagement, making it ideal for someone who understands both clinical-stage bioprocessing and the practical realities of GMP manufacturing. You'll work closely with Development, Manufacturing, QA, QC, Bioengineering, Procurement, and external customers to ensure successful technology transfer and operational delivery.
What You'll Be Responsible For:
Technology Transfer & MSAT Leadership
Lead the transfer of development processes into GMP manufacturing facilities Act as the primary technical point of contact for customers throughout technology transfer projects Ensure new processes are robust, scalable, and suitable for GMP manufacture Coordinate activities across Process Development, Manufacturing, QA, QC, Bioengineering, and external stakeholders to ensure successful implementation
GMP Manufacturing Support
Manage the day-to-day delivery of manufacturing support and preparation activities Ensure production activities are executed safely, compliantly, and to schedule Support the introduction of new products and processes into manufacturing operations Lead deviation investigations, impact assessments, CAPAs, and technical reviews associated with transferred processes
People Leadership
Lead a small operational team, including GMP operators and manufacturing support personnel Set objectives, manage performance, and support development of team members Ensure appropriate training, competency, and resource planning to support manufacturing activities Foster a culture of collaboration, accountability, and continuous improvement
Cross-Functional Project Leadership
Lead complex multidisciplinary projects involving technical, operational, and quality functions Coordinate delivery across multiple stakeholders and competing priorities Support strategic resource, capacity, and equipment planning Ensure projects are delivered on time, to budget, and to required quality standards
Customer & Business Engagement
Work directly with customers to support process transfer and manufacturing readiness Contribute technical expertise to business development activities and proposal development Support future work-winning activities through technical input and customer engagement Build strong relationships internally and externally to support successful project delivery
About You
You are an experienced bioprocessing or manufacturing professional who enjoys working across multiple functions and taking ownership of complex technical programmes.
You'll bring:
Significant experience within bioprocessing, biologics manufacturing, or MSAT environments Strong understanding of GMP manufacturing and quality systems Experience transferring development processes into clinical or GMP manufacturing environments Knowledge of upstream, downstream, and analytical bioprocessing activities Experience leading technical projects and coordinating cross-functional teams Strong problem-solving capability and the confidence to make decisions in complex environments Excellent stakeholder management and customer-facing skills
Highly desirable:
Clinical-stage manufacturing experience MSAT, process transfer, or process validation experience Experience managing GMP operators or production teams Knowledge of biologics manufacturing and CMC principles Experience within mRNA, RNA therapeutics, or advanced biologics environments Project management experienceWhy Join Us?
Opportunity to play a pivotal role in the transfer of innovative products into GMP manufacture Lead technically complex, customer-facing projects Combine scientific, operational, and leadership responsibilities Be part of a growing manufacturing organisation supporting cutting-edge therapies Competitive salary package of up to £70,000Location & Working Pattern
Based in Darlington Full-time permanent position Primarily site-based due to manufacturing and operational activities Flexible working arrangements available around core business requirementsThe Opportunity
This is an outstanding opportunity for an experienced GMP or bioprocessing professional to step into a role that sits at the heart of manufacturing delivery. You'll combine technical expertise, customer engagement, technology transfer, and people leadership to ensure innovative therapies successfully move from development into GMP production.
Guidant, Carbon60, Lorien & SRG - The Impellam Group Portfolio are acting as an Employment Business in relation to this vacancy Only candidates based in UK and eligible to work in UK are allowed
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