LSC have a great contract opportunity for a HVAC and Cleanroom CQV 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 previous experience in biopharmaceutical manufacturing and are ready for your next challenge, this could be the perfect project for you
ABOUT THE PROJECT - KEY RESPONSIBILITIES:**
Prepare and execute the site commissioning and validation testing for HVAC & Clean Rooms at the manufacturing facility in alignment with site and global company procedures.
* Responsible for meeting key project deliverables for safety, CQV schedule management and quality of project related documentation/electronic records for HVAC & Clean Rooms assigned.
* Responsible for ensuring GMP Clean Rooms, Cold Rooms and HVAC Equipment systems are tested in compliance with good manufacturing practices, company policies and EU & FDA regulations.
* Responsible for ensuring that all non GMP HVAC and systems are tested in compliance with project related standards from a commissioning perspective.
* Deviation management associated with the assigned HVAC & Clean Rooms.
ARE YOUR SKILLS A MATCH?
* Hold a minimum of a BS qualification (Degree) in a scientific, technical or engineering discipline along with a minimum of 3-5 years of experience within the pharmaceutical industrial ideally with familiarity with Sterile Drug Product filling line experience.
* Demonstrable capacity to implement a project CQV strategy, effectively execute the CQV testing approach for assigned from initiation to completion.
* CQV project lifecycle experience from end-to-end design through to C&Q and handover.
* Understands the project management process; programming, scope development, design development, implementation, and project closeout.
* 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 CQV of Drug Substance/Drug product sterile manufacturing HVAC & Clean Rooms with integrated automation platforms.
Please apply directly via this advert or contact Stephen Abdullah on to discuss this opportunity in more detail.
All applicants must have a valid work permit for at least 12 months. LSC cannot offer work permit or visa sponsorship.