Cells Senior Technician
London, England, United Kingdom Full-time Posted 5 days ago
THE POSITION
The Cells Senior Technician plays a key role in upstream production by contributing to the large-scale manufacture of cells used in antigen production. Working as part of a technical team, this position ensures production activities are carried out safely, efficiently, and in line with GMP, biosafety and HSE requirements. The role combines hands-on laboratory work with responsibility for documentation, process improvement, and support during audits, contributing directly to the continuity and quality of manufacturing operations.
This is a fixed-term contract until 31st December 2027.
Tasks And Responsibilities
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies.
To learn more about why BI is a great place to work, visit:
https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Our Company
Why Boehringer Ingelheim?
With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.
Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
Want to learn more? Visit https://www.boehringer-ingelheim.com
The Cells Senior Technician plays a key role in upstream production by contributing to the large-scale manufacture of cells used in antigen production. Working as part of a technical team, this position ensures production activities are carried out safely, efficiently, and in line with GMP, biosafety and HSE requirements. The role combines hands-on laboratory work with responsibility for documentation, process improvement, and support during audits, contributing directly to the continuity and quality of manufacturing operations.
This is a fixed-term contract until 31st December 2027.
Tasks And Responsibilities
- Execute production operations in accordance with defined procedures and ensure product quality and integrity
- Operate and maintain laboratory areas to cleanroom standards required for production
- Maintain accurate and contemporaneous production batch records
- Contribute to the manufacture of cells in compliance with EU, UK and company GMP, Biosafety and HSE regulations
- Identify and implement process improvements through the change control system
- Provide technical guidance and training to other team members when required
- Participate in area monitoring and call-out rota for operational support
- Support EHS activities, including reporting incidents, participating in investigations, and completing risk assessments
- Monitor and support cost centre activities, including reviewing spend and reporting discrepancies
- Perform transactional activities such as stock movements, invoice approvals and purchasing via relevant systems (e.g. SAP, WeBuy)
- Raise and manage CAPAs, deviations, change controls and out-of-specification investigations
- Ensure accurate documentation and provide required information to Quality Assurance
- Collaborate with other production departments and stakeholders to support manufacturing activities
- Ability to follow detailed technical procedures accurately and consistently
- Strong attention to detail with a methodical approach to tasks
- Ability to plan and manage workload effectively to meet production schedules
- Good written and verbal communication skills
- Willingness to work in a controlled laboratory environment and participate in rota-based coverage, including occasional weekend support
- Knowledge of GMP and regulated laboratory practices, including documentation standards
- Good working knowledge of Microsoft Office applications (Word, Excel, Outlook)
- Secondary education (or equivalent) including Mathematics and English
- Demonstrated behaviours aligned with accountability, agility and continuous improvement
- Positive and proactive approach to problem solving and collaboration
- Experience working in a pharmaceutical, biotechnology, or otherwise highly regulated production environment is preferred
- Experience supporting audits, deviation investigations, CAPAs or change control processes, as well as familiarity with laboratory systems and tools (LIMS, SAP or similar systems) is beneficial
WHY THIS IS A GREAT PLACE TO WORK
Boehringer Ingelheim has been recognised as a Top Employer in the UK, demonstrating our commitment to building an exceptional workplace through strong people practices and supportive HR policies.
To learn more about why BI is a great place to work, visit:
https://www.boehringer-ingelheim.co.uk/careers/uk-careers/why-great-place-work
Our Company
Why Boehringer Ingelheim?
With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.
Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.
Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.
Want to learn more? Visit https://www.boehringer-ingelheim.com
