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 021 4718212 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.
