Validation Engineer Role Denmark

CQV Buffer Engineer

  • Posted Mar 2, 2023
  • Denmark
  • Contract
  • BBBH26275

LSC has a fantastic opportunity for CQV Buffer Engineer to join an advanced global team in Denmark that promotes self-development, encourages collaboration, and fosters a learning environment.

The company specialises in clinical & commercial manufacturing of Biotech medicines, including viral gene therapies and has built a strong reputation over the years for bringing complex and lifechanging therapies into reality.

Role Functions:

  • Support the commissioning, qualification and validation of buffer prep systems and equipment as part of the Drug Substance expansion.
  • Ensure commissioning readiness of all systems to support equipment start-up and IOQ testing.
  • Conduct predominantly SAT activities aligned to the current equipment vendor during installation and readiness.
  • Liaise with all Project Groups and the CQV Document Generation Lead.
  • Support execution of all LSCC CQV deliverables; IOQ, field execution.
  • Generate and ensure timely approval of all commissioning and IOQ final reports.

Experience, Knowledge & Skills:

  • 10 years' experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
  • Experience within media prep, buffer prep and / or buffer hold.
  • Previous experience of delivering FAT/SAT activities.
  • Capacity to keep work pace and meet deadlines.
  • Excellent planning and organising abilities.

Qualifications & Education:
Bachelor Degree or higher preferred: ideally in an Engineering related discipline.

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The benefits of contracting with LSC

  • Partners to the world’s top Life Science companies we offer you the best contract opportunities in the industry
  • 95% of LSC contracts are renewed letting you choose contracting as a long term career option
  • LSC’s Consultant Success Programme focuses on skills development & on-site support to help you achieve your career goals!

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