(11/7/2025 A) Inspection C&Q Engineer

3 weeks ago

Dublin, Ireland Life Science Consultants (LSC) Full time

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 if you have any more questions about this role Skills: commissioning cqv inspection vial syringe filling

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