Overview
In this role you will support the aseptic manufacture, dispensing and packaging of clinical products within a GMP-regulated setting. You will work as part of a skilled team to ensure products meet high quality, safety, and regulatory standards. You will handle documentation and material management, contributing to process development and continuous improvement. This position offers exposure to clinical supplies and pharmaceutical development in a compliant, safety-focused environment.
Pay / Benefits
- Salary
Responsibilities
- Manufacture, dispense and package clinical products per GMP and company procedures
- Prepare and complete manufacturing and supply documentation
- Dispense APIs, excipients, drug products, IMPs and packaging materials
- Maintain GMP stock levels and assist with ordering, receipt, storage and stock control
- Support cleaning, maintenance and upkeep of GMP facilities, utilities and equipment
- Record work accurately in line with regulatory and client requirements
- Support process development studies and non-clinical batch manufacture as needed
- Collaborate with Quality Control, microbiology and purchasing for material management
- Follow health and safety procedures at all times
- Be flexible to work across the site to meet business and client needs
Key requirements
- BSc or equivalent in a relevant scientific discipline
- Good written and verbal communication
- Strong attention to detail and ability to follow procedures
- Ability to work in a regulated environment emphasizing documentation, quality and compliance
- Organised with multitasking and prioritisation
- Positive, flexible attitude to new work challenges
- Commitment to health, safety and GMP standards
- Experience in a GMP-regulated facility or GMP manufacturing environment
- detail-oriented
- organised
- flexible
- GMP manufacturing experience
- aseptic manufacturing
- knowledge of APIs, excipients, IMPs or clinical packaging materials
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