CQV Lead
- Denmark
- Contract
- Commissioning, Qualification and Validation
Our client, a global biopharmaceutical manufacturing organisation, is recruiting for a CQV Lead to join them on their new expansion project. Based in a charming Nordic location, this is on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
Responsibilities:
- CQV Lead Engineer for the HVAC systems initially responsible for timely review and approval of all CQV documentation, including but not limited to – EDR-DQ, SIA, FAT, RTM, QRA, RV, SAT, IOC, IOQ and Final Reports.
- Review of all Design deliverables from EPCM, including Drawings, Datasheets, specifications and Engineering Lists. Also assist in GMP reviews.
- Review of all GMP-generated documentation.
- Minimum of 10 - 15 years’ experience including experience with design and construction projects for biopharmaceutical manufacturing facilities.
- Experience with complex projects and within a CQV Lead capacity taking responsibility for a team of engineers.
The candidate must have the rights to work in the location stated in the job advert.
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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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