Senior GMP Manufacturing Supervisor
3 weeks ago
About eXmoor Pharma Concepts Limited
">eXmoor Pharma Concepts Limited is a renowned company providing comprehensive services in cell and gene therapies (CGT) and biopharmaceuticals. Our mission is to support clients with their manufacturing needs, from translation consultancy to capital project design, licensing, and GMP manufacturing for early phase clinical trials.
We are seeking an experienced GMP Production Facility Manager to join our team. This role offers a unique opportunity to work on various client projects in a rapidly growing business while developing your quality management career.
">About the Role
">- The successful candidate will lead and develop the GMP production team, responsible for the day-to-day management, operation, scheduling, and administration of the GMP facility, ensuring it is operated and maintained as required by the facility's licenses.
- You will be named as Production Manager on the GMP Facility's Manufacturing Authorisation, responsible for leading the GMP team & qualification of the facility, equipment, and processes.
- You will ensure that products are produced and stored according to authorised specifications.
Main Responsibilities
">- Manufacturing Licence: You will be responsible for all aspects of the facility, including maintenance, operation, qualification, validation, material storage, and waste, ensuring all are managed in compliance with the facility's stated procedures and standards.
- People: You will recruit, train, develop, and lead production staff to meet planned production needs and departmental budgets, establishing a motivated, capable team.
- Production Planning: You will lead and manage all aspects of production planning, including resource allocation, budgeting, progress reporting, and forecasting.
Requirements
">- MSc in Life Science or BSc with relevant years of industry experience or equivalent experience.
- Considerable experience (5 years plus) of managing GMP clean room facilities, production, facility, and equipment qualification, quality, and GMP documentation.
- In-depth understanding of the legislative framework of MHRA, HTA, and H&SE in Good Manufacturing Practice as applied to small-scale biopharmaceutical production for clinical trials.
- Significant experience in a supervisory or management role, including the ability to lead, develop, motivate, and organise a small team.
Estimated Salary: £60,000 - £80,000 per annum
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