VP Cross-Functional Shift Technician

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

The Virus Production Cross-Functional Shift Technician is a key role within Manufacturing, responsible for participating in the production of bulk volumes of inactivated Foot and Mouth Disease (FMD) and Blue Tongue Virus (BTV) antigens used in vaccine manufacturing. This is a cross-functional position supporting two Virus Production teams (VP1 and VP2). The successful candidate will be required to work across both areas based on business and departmental needs, providing flexibility and support where operational demand requires. The role involves collaborating with teams across the site to support performance, quality, and continuous improvement within a shift-based environment. This is a fully site-based position in Pirbright, offered on a fixed-term contract until 31 December 2027.

TASKS & 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

EHS & Compliance

• Report and support investigation of EHS incidents
• Perform and document risk assessments
• Complete all assigned Health & Safety training
• Ensure full compliance with GMP, biosafety, and regulatory requirements
• Good standard of education (including Maths and English)

Skills & Experience

• 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)

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 DB