Virus Production Shift Technician (Pirbright, United Kingdom, Surrey)
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THE POSITION
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.
Learn more about why BI is a great place to work:
https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
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.
Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 3428 comparable Manufacturing & CMC roles across 175 biopharma companies.
Salary context
813 of 3428 peers report a salary range (USD, annualized)
Peers share this role's job function. This posting doesn't list a seniority level, so peers aren't narrowed by seniority either -- the range below may span more levels than usual.
Where these roles are based
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Seniority mix
1516 of 3428 peers have a known seniority level
Therapeutic area mix
22 of 3428 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
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Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
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