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Westmeath
Republic of Ireland
Galway
Cork
Dublin
Dublin
Cork
Dublin
Galway
Galway
Carlow
Limerick
Wexford
Galway
Dublin
Galway
Dublin
Republic of Ireland
Dublin
Galway
Tipperary
Cork
Tipperary
Tipperary
Dublin
Dublin
Louth
Carlow
Dublin South
Galway
Galway
Galway City
Dublin
Galway
Limerick
Carlow
Dublin
Dublin
Galway
Dublin
Wexford
Dublin
Limerick
Galway
Galway
Galway
Dublin
Limerick
Limerick
Galway
Dublin
Galway
Galway
Galway City
Galway
Tipperary
Galway
Galway
Republic of Ireland
Limerick City
Dublin
Republic of Ireland
Dublin
Carlow
Tipperary
Westmeath
Galway
Westmeath
Cork
Dublin
Limerick
Limerick
Galway
Dublin
Limerick
Limerick
Dublin
Galway
Limerick
Dublin
Galway
Carlow
Galway
Tipperary
Galway
Dublin
Galway
Dublin
Dublin
Limerick
Galway
Cork
Limerick
Dublin
Galway
Cork
Dublin
Waterford
Midlands
Galway
Galway
Dublin
Westmeath
Limerick
Dublin
Galway
Dublin
Republic of Ireland
Dublin
Cork
Cork
Limerick
Limerick
Republic of Ireland
Dublin
Dublin
Limerick
Limerick
Cork
Galway
Donegal
Tipperary
Tipperary
Dublin
Westmeath
Carlow
Clare
Limerick
Commissioning and Qualification Engineer
| Reference: | SMC475695 | Location: |
Dublin |
| Qualification: | Degree | Experience: | See description |
| Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
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
· Coordinates and Supervises all C&Q activities.
· Generate 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)
· Manages Daily C&Q coordination meetings.
· Responsible for Overall Tracking and Reporting of C&Q status and risks/issues.
· Ensures Startup of equipment/utilities is completed in a safe and coordinated manner.
· Assist 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.
If interested in this posting please feel free to contact Seán McCarthy on +353 (0)87 798 8480 or [email protected] for further information.
Life Science Recruitment | Tel:+353 1 685 4848 | Fax: +353 (0)1 443 05 24 | Email: [email protected] | Copyright © 2021 Life Science Recruitment Ltd
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