THE POSITION
Production Services and Formulation Technician is a key role within Manufacturing Operations, responsible for supporting production-related activities across the Pirbright manufacturing facility. The role enables the large‑scale production of Foot and Mouth Disease (FMD) and Blue Tongue Virus (BTV) antigens, as well as finished vaccine products, in a timely and cost‑effective manner.
Working across production services, formulation and operational support areas, the Technician plays an important role in ensuring product quality, equipment readiness and smooth execution of manufacturing processes, while contributing to continuous improvement initiatives across the site.
This is a fixed‑term contract until December 2027 and a fully site‑based position in Pirbright.
Tasks & Responsibilities
- Execute production operations across formulation, antigen control and production services in line with defined procedures and quality standards
- Perform equipment preparation, cleaning and sterilisation activities, including operation of autoclaves and routine testing cycles
- Support antigen formulation activities, including preparation of trial blends and handling of materials such as liquid nitrogen and dry ice
- Carry out product filling and related operations, ensuring product quality, sterility and compliance
- Ensure accurate completion of manufacturing documentation in line with GMP, GDP and data integrity requirements
- Support labelling, receipt, storage and transfer of materials and products, including SAP transactions
- Maintain stock levels and ensure materials are managed in line with storage and expiry requirements
- Support preparation and delivery of production equipment (e.g. sterile glassware, bottles) to operational areas
- Participate in gowning qualifications, aseptic simulations and required training activities
- Contribute to continuous improvement initiatives, including participation in Tier 1 meetings and implementation of 5S principles
- Support updates to SOPs and provide input into process improvements
EHS & Compliance
- Report and support investigation of EHS incidents and safety observations
- Perform and document risk assessments as required
- Complete assigned Health & Safety training
- Ensure full compliance with GMP, biosafety, HSE and regulatory requirements
- Support audit readiness and participate in internal and external inspections
- Assist with deviations, CAPA activities and change controls where required
Requirements
Education
- Minimum of 5 GCSEs including English, Maths and Science (Grade 4/C or above)
- Degree in a scientific discipline is preferred, or equivalent experience in a relevant environment
Skills & Experience
- Experience in a pharmaceutical, biotechnology or other regulated manufacturing environment
- GMP experience is essential
- Knowledge of HSE, biosafety standards and operational excellence principles
- Experience with production documentation and systems (e.g. SAP, LIMS) is desirable
- Ability to plan and manage work effectively to meet deadlines
- Strong organisational and communication skills
- Ability to work both independently and as part of a team
- Strong attention to detail and ability to follow procedures accurately
- Problem‑solving mindset with the ability to suggest improvements
- Positive, proactive and can‑do attitude
- Good IT skills (e.g. Microsoft Office)
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