Vaccine Manufacturing Shift Technician

Vaccine Manufacturing Shift Technician

Full-Time 24750 - 30250 Β£ / year (est.) No working from home possible
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At a Glance

  • Tasks: Support vaccine production and maintain cleanroom conditions in a regulated environment.
  • Company: Boehringer Ingelheim, a leader in biopharmaceuticals.
  • Benefits: Full-time role with competitive pay and valuable experience in the biotech field.
  • Other info: Fixed-term role until December 2027 with potential for growth.
  • Why this job: Join a mission-driven team making a difference in public health.
  • Qualifications: No specific experience required; just a passion for science and teamwork.

The predicted salary is between 24750 - 30250 Β£ per year.

Boehringer Ingelheim UK is seeking a Virus Production Shift Technician to support the production of FMD antigen in a regulated manufacturing environment at the Pirbright site.

The role is full-time, fixed-term until 31 December 2027, with shift-based work that may include nights, weekends, and non-standard hours.

You will execute manufacturing activities, perform CIP/SIP, maintain cleanroom conditions, document batch records, manage materials, and support CAPA and deviation investigations.

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Vaccine Manufacturing Shift Technician employer: Boehringer Ingelheim

Boehringer Ingelheim in Pirbright offers a dynamic work environment where innovation and compliance are at the forefront of our operations. As a leading player in the pharmaceutical industry, we provide our employees with robust growth opportunities, a supportive culture that values teamwork, and a commitment to quality that empowers you to make a meaningful impact. Join us and be part of a company that prioritises your professional development while contributing to the health and well-being of communities worldwide.

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Contact Details:

Boehringer Ingelheim Recruitment Team

We think you need these skills to ace Vaccine Manufacturing Shift Technician

Manufacturing Activities Execution
CIP/SIP Procedures
Cleanroom Maintenance
Batch Record Documentation
Material Management
CAPA Support
Deviation Investigation