CQV Lead
- Cork
- Contract
- Commissioning, Qualification and Validation
This vacancy has now expired
I am working with a leading Biopharmaceutical company and due to a large capital investment are looking to expand upon their existing manufacturing facility. To support this expansion I am looking for an experienced CQV Lead who will work within their existing team. The succesful individual will have the opportunity to work within a fully automated state of the art facility and help support the Commissioning and Qualification of equipment, processes and methodologies.
The Contract is for an initial period of 12 months however the contract is likely to extend for up to 24 months.
The CQV Lead will be responsible for:
- Developing receipt verification forms and installation verification protocols.
- Execute test cases.
- Provide technical oversight.
- Train staff as required to support commissioning.
- Work closely with CQ Manager to facilitate the completion of CQ work.
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I have always received a highly professional & personable service from the team at Quanta. They listen carefully to the specific requirements of available roles and work tirelessly to supply a pool of potential candidates and make the hiring and contract renewal process an easy activity to manage.
Global Pharmaceutical firm
Once again can I via you recognise the superb support I was given before, during and after this short contract. The support, was as usual professional and every friendly.
QA Specialist
We have worked together with Quanta for seven years now and have always received a professional service. Quanta’s speciality certainly lies within their technical sourcing abilities and they have met our demanding requirements time and time again. Coupled with this are the integrity of Quanta’s people and their ability to deliver.
Global Pharmaceutical firm
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Amy
I manage this role.