Only 24h Left: Commissioning and Qualification Engineer
4 weeks ago
We're currently recruiting for an exciting opportunity with an award-winning biopharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties
1. Coordinates and supervises all C&Q activities.
2. Generates C&Q planning documents detailing overall strategy for the project.
3. Develops the master list of C&Q test documents and activities.
4. Generates all C&Q summary reports.
5. Ensures the C&Q schedule is developed and maintained.
6. Generation of all C&Q test documents (C&Q Plan/Set to Works/FAT/SAT/IV/FT/C&Qsr).
7. Manages daily C&Q coordination meetings.
8. Responsible for overall tracking and reporting of C&Q status and risks/issues.
9. Ensures startup of equipment/utilities is completed in a safe and coordinated manner.
10. Assists in the development of User Requirement Specifications (URS's) and Quality.
Education & Experience
1. 6+ years experience in Engineering or Commissioning and Qualification Management.
2. Technical qualification at third level or equivalent in Engineering.
3. Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects.
4. Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
5. Knowledge of safety, GMP and environmental regulatory requirements.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or sean.mccarthy@lifescience.ie for further information.
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