C&Q Engineer Role Dublin

Inspection C&Q Engineer

  • Posted Today
  • Dublin
  • Contract
  • BBBH28575

LSC have a great contract opportunity for a C&Q Engineer to join a Dublin based Biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that can help patients overcome serious diseases and improve their quality of life.

If you have 5 years of experience in C&Q in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you!

ABOUT THE PROJECT - KEY RESPONSIBILITIES:
Working with drug product Area CQV Lead prepare and execute the site commissioning and validation testing for equipment utilities in alignment with site and global procedures.
RESPONSIBLITIES:

  • Development and execution of CQV testing documentation for Inspection Systems including Syringe and Vial Automated Visual Inspection Equipment and Manual Inspection Booths for the Sterile Drug product facility.
  • Responsible for meeting key project deliverables for safety, CQV schedule and quality of project related documentation/electronic records for equipment, utilities assigned.
  • Responsible for ensuring GMP equipment are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
  • Deviation management associated with the assigned equipment and utilities.

ABOUT YOU - ARE YOUR SKILLS A MATCH?

  • Minimum of a BS qualification (Degree) in a scientific, technical or engineering discipline along with a minimum of 5 years of experience within the pharmaceutical industrial ideally with familiarity with Sterile Drug Product filling line experience.
  • CQV project lifecycle experience from design through to C&Q and handover.
  • Demonstrable experience of performing as part of diverse team of CQV professionals/ contractors to deliver on tasks safely, with quality focus, on time and within budget.
  • Experience in leading, managing and execution of FAT activities.
  • Solid background of document preparation, execution, and task planning on CQV projects with a demonstrated record of on time performance.
  • Previous experience with electronic validation platform (e.g. ValGenesis, Kneat).

Note: Are you currently eligible to work in Ireland? As this is a contract opportunity you will need to hold a Stamp 1G/Stamp 4 visa to apply!

Apply via this advert or contact LSC on 021 4777329 if you have any more questions about this role!

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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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