The Virus Production Shift Technician plays an important role within Manufacturing, supporting the production of Foot and Mouth Disease (FMD) antigen used in vaccine manufacturing. The role is based within a highly regulated and technically advanced manufacturing environment, contributing to the delivery of critical vaccine materials while supporting operational excellence and continuous improvement initiatives.
This is a fully site-based, fixed-term role in Pirbright until 31 December 2027, operating within a shift-based manufacturing environment. Details of the shift pattern will be communicated at a later stage. The role may involve night shifts, weekend working, and other non-standard hours in line with operational requirements.
TASKS & RESPONSIBILITIES
- Execute manufacturing activities in line with approved procedures, GMP standards, and production schedules
- Perform CIP (Clean-In-Place) and SIP (Sterilise-In-Place) operations to support production activities
- Operate and maintain cleanroom and laboratory environments in accordance with regulatory requirements
- Accurately complete batch records and manufacturing documentation
- Manage raw material inventories and perform routine stock control activities
- Operate autoclaves and perform cleaning, sterilisation, and testing activities
- Carry out Grade A/B aseptic processing and work within Biosafety Cabinets (BSCs)
- Follow Standard Operating Procedures (SOPs) and complete all required training
- Support production investigations, including deviation management and root cause analysis
- Assist with CAPA activities and implementation of corrective actions
- Participate in daily Tier 1 meetings and contribute to team performance objectives
- Support continuous improvement initiatives across the manufacturing operation
- Provide flexible support for out-of-hours production activities when required
EHS & Compliance
- Ensure compliance with GMP, Biosafety, Biosecurity, and Health & Safety requirements
- Report and support investigations relating to EHS incidents
- Perform and document risk assessments
- Complete mandatory Health & Safety training
- Promote safe working practices and maintain a strong compliance culture
REQUIREMENTS
Education
- Good standard of education, including Maths and English
- Scientific, technical, or manufacturing-related qualifications are advantageous
Skills & Experience
- Experience working in a pharmaceutical, biotechnology, vaccine, or other highly regulated manufacturing environment
- Understanding of GMP principles and quality requirements
- Experience working in cleanroom environments is desirable
- Experience with aseptic processing or sterile manufacturing operations would be advantageous
- Knowledge of deviation management and CAPA processes is beneficial
- Strong attention to detail and commitment to quality
- Ability to follow detailed procedures and maintain accurate documentation
- Good organisational and time management skills
- Strong communication and teamwork skills
- Competent IT skills, including Microsoft Office applications
- Proactive approach and ability to work independently when required
- Flexibility to adapt to changing production priorities and operational needs
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim is recognised as a Top Employer in the UK , reflecting our commitment to exceptional workplace standards, career development and a purpose-driven culture. Our employees contribute to meaningful work, creating long-term value for people, animals and the environment.
Candidates may be asked to undergo a Basic Disclosure and Barring Service (DBS) Security check. Any offer of employment will be subject to satisfactory DBS certificate.
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