Cqv Technician

Lonza Group

Slough, United Kingdom
Not specified (assumed to be hybrid or onsite based on industry norms).
Commissioning qualification and validation execution
Cgmp standards compliance knowledge
Manufacturing systems and equipment support
Lonza Group is seeking a CQV Technician for their Slough facility, responsible for executing commissioning, qualification, and validation protocols for biopharmaceutical manufacturing. The role emphasizes collaboration across teams and adherence to cGMP standards, while offering opportunities for career development in an inclusive workplace

Job Summary

  • You will play a hands-on role in commissioning and qualifying critical systems and equipment contributing directly to the delivery of high-quality medicines.
  • The role requires maintaining strict compliance with cGMP standards, internal procedures, and training requirements within a regulated environment.
  • Candidates will collaborate with Manufacturing, Laboratories, and Technical Services to ensure alignment of CQV activities and meet quality standards.

Matching Summary

Match Score: 85

Lonza Group is seeking a CQV Technician for their Slough facility, responsible for executing commissioning, qualification, and validation protocols for biopharmaceutical manufacturing. The role emphasizes collaboration across teams and adherence to cGMP standards, while offering opportunities for career development in an inclusive workplace.

Skills & Requirements

Must-have

  • Commissioning qualification and validation execution
  • cGMP standards compliance knowledge
  • Manufacturing systems and equipment support

Nice-to-have

  • Strong analytical mindset with attention to detail
  • Proactive approach to continuous improvement
  • Ability to collaborate across multiple teams

Key Requirements

  • Degree in Engineering or Life Sciences
  • Experience in regulated pharmaceutical or biotech environments
  • Understanding of quality systems and cGMP

Work Rights

Not specified

Tailored Resume

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