Commissioning and Qualification Engineer
We are currently seeking an experienced Commissioning and Qualification Engineer to join our team at {company}, a leading biopharmaceutical organization based in Cork.
This is an excellent opportunity for individuals who are looking to work with a multinational company that is renowned for its excellence in the industry.
Duties:
* Coordinates and supervises all C&Q activities.
* Generates C&Q planning documents detailing overall strategy for the project.
* Develops the master list of C&Q test documents and activities.
* Generates all C&Q summary reports.
* Ensures the C&Q schedule is developed and maintained.
* Generation of all C&Q test documents (C&Q Plan/Set to Works/FAT/SAT/IV/FT/C&Qsr).
* Ensures startup of equipment/utilities is completed in a safe and coordinated manner.
* Assists in the development of User Requirement Specifications (URS's) and Quality.
Education & Experience:
* 6+ years experience in Engineering or Commissioning and Qualification Management.
* Technical qualification at third level or equivalent in Engineering.
* Extensive knowledge and demonstrated experience managing Commissioning and Qualification for Pharmaceutical / Biotechnology projects.
* Experience of sterile / biotech equipment within the pharmaceutical industry is preferred.
* Knowledge of safety, GMP and environmental regulatory requirements.
Salary:
$120,000 - $150,000 per year, depending on experience.