Shift Virus Production Technician (Cross-Functional, GMP)

Boehringer Ingelheim; Guildford; On-site; GBP 28,000 - 36,000; Full time

Job summary

Boehringer Ingelheim is seeking a Virus Production Cross-Functional Shift Technician to support two virus production teams (VP1 and VP2) at Pirbright. The role covers manufacturing ops, cleanroom management, batch documentation, and GMP compliance in a cross-functional, shift-based setting.

The successful candidate will work across site teams, contribute to CAPAs and deviations, and support audits while maintaining high accuracy in data entry and documentation in LIMS/SAP.

Qualifications

• Experience in a pharmaceutical, biotechnology, or regulated manufacturing environment.
• Experience working in cleanroom environments (Grade A/B preferred).
• Knowledge of GMP, biosafety, and quality standards.
• Experience in aseptic or tissue culture processes is desirable.
• Experience with deviation handling and documentation systems (e.g. LIMS, SAP) is an advantage.
• Ability to follow detailed procedures and work with a high level of accuracy.
• Strong organizational and time management skills.
• Ability to work independently and as part of a team.
• Good verbal and written communication skills.
• Proactive, reliable, and structured approach with a positive attitude.
• Basic IT skills (e.g. Microsoft Office)

Responsibilities

• Execute production operations in line with defined procedures and quality standards
• Operate and maintain laboratory and cleanroom environments (Grade A-D) to required standards
• Complete batch records and production documentation accurately and in a timely manner
• Maintain raw material stocks, including routine stock checks
• Perform manufacturing activities, including cell culture processes where required
• Follow and implement Standard Operating Procedures (SOPs) and complete required training
• Generate deviations and support investigations, including CAPA activities
• Support audit readiness and collaborate with QA during internal and external audits
• Complete data entry and manage documentation within systems such as LIMS and SAP
• Participate in Tier 1 meetings and ensure actions are completed within agreed timelines
• Contribute to continuous improvement initiatives within the production area

Skills

Pharma manufacturing

Cleanroom experience

GMP/biosafety

Aseptic culture

Deviation handling LIMS SAP

Attention to detail

Time management

Teamwork/independence

Communication skills

Proactive attitude

MS Office

Job description

Boehringer Ingelheim is seeking a Virus Production Cross-Functional Shift Technician to support two virus production teams (VP1 and VP2) at Pirbright. The role covers manufacturing ops, cleanroom management, batch documentation, and GMP compliance in a cross-functional, shift-based setting.

The successful candidate will work across site teams, contribute to CAPAs and deviations, and support audits while maintaining high accuracy in data entry and documentation in LIMS/SAP.