VP Cross-Functional Shift Technician

Boehringer Ingelheim GmbH; United Kingdom; Remote; GBP 26,000 - 36,000; Full time

Job summary

Boehringer Ingelheim GmbH in Pirbright, UK, is seeking a Virus Production Cross-Functional Shift Technician to support two virus production teams (VP1 and VP2) in producing bulk quantities of inactivated FMD and BTV antigens, ensuring quality and compliance in a shift-based environment.

This is a site-based, fixed-term role until 31 December 2027, with opportunities to contribute to continuous improvement, CAPA activities and QA collaboration within GMP and biosafety standards.

Qualifications

• Experience in a pharmaceutical/regulated manufacturing environment.
• Cleanroom experience (Grade A/B preferred).
• Knowledge of GMP, biosafety, and quality standards.
• Aseptic or tissue culture processes desirable.
• Experience with deviation handling and documentation systems (LIMS, SAP) advantageous.
• Ability to follow detailed procedures with high accuracy.
• Strong organizational and time management skills.
• Good verbal and written communication skills.
• Proactive, reliable and structured approach.

Responsibilities

• Execute production operations in line with procedures and quality standards.
• Operate and maintain cleanroom environments (Grade A–D) to required standards.
• Complete batch records and production documentation accurately.
• Maintain raw material stocks with routine stock checks.
• Perform manufacturing activities, including cell culture processes where required.
• Follow SOPs and complete required training.
• Generate deviations and support investigations, including CAPA activities.
• Support audit readiness and collaborate with QA during audits.
• Complete data entry and manage documentation in LIMS and SAP.
• Participate in Tier 1 meetings and ensure actions are completed on time.
• Contribute to continuous improvement initiatives within production area.

Skills

Pharma/manufacturing experience

Cleanroom experience

GMP/biosafety knowledge

Documentation (LIMS/SAP)

Procedural accuracy

Teamwork/communication

Education

Good standard of education (Maths & English)

Tools

LIMS

SAP

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

REQUIREMENTS

Education

• 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)

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 DB