Description
C&Q specialist required to join a pharmaceutical company in central Ireland. The Commissioning and Qualification Engineer will be responsible for supporting a number of PV batches for an initial 3 month contract.Role and responsibilities:
* Strong experience in the facility and GMP utility commissioning and qualification
* Strong experience in qualifying manufacturing process automation systems
* Strong experience in equipment commissioning qualification
* Experience and participation in HPRA/IMB audits
* Experience operating in a Manufacturing or Operations environment
* Understanding of Pharmaceutical Manufacturing Processes
* Strong experience and working acknowledge of quality systems including Deviation and CAPA generation, investigation and resolution
* Ability to assess impact of changes to direct and indirect systems during commissioning activities
* Ability to co-ordinate and lead commissioning and qualification activities against project schedule and report to the validation lead and head of quality
* Ability to resolve validation and qualification exceptions/deviations
* Ability to liaise with cross functional teams and other contracting resources
* Ability to direct and articulate quality requirements and represent the client in the achievement of compliant and qualified systems.
* Strong communication skills
If this is you please apply today.