LSC have a great contract opportunity for a CQV Equipment 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.
ABOUT THE PROJECT - KEY RESPONSIBILITIES:
- Development and execution of CQV testing documentation for Utilities 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 and utilities assigned.
- Responsible for ensuring Utilities are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
- Responsible for ensuring that all non GMP equipment Utilities are tested in compliance with project related standards from a commissioning perspective.
ABOUT YOU - ARE YOUR SKILLS A MATCH?
- The ideal candidate should hold a minimum of a BS qualification (Degree) in a scientific, technical or engineering discipline.
- Minimum of 5 years of experience with utility systems commissioning preferably in a sterile drug product facility.
Applicants interested in our contracting opportunities within the pharmaceutical sector in Ireland are required to have a Stamp 1G or a Stamp 4 visa. Please understand that we are unable to provide visa sponsorship.
Apply via this advert or contact Cian Murnane on 021 4777 329 if you have any more questions about this opportunity!
