CQV Engineer
- Denmark
- Contract
- Life Sciences
This vacancy has now expired
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CQV Engineer to join them on their new expansion project. Based in a charming Nordic location, this on a contractual basis, and will involve significantly growing the sites capacity for the manufacture of Biologics.
As CQV Engineer, you will be responsible for the delivery of CQV Engineer activities on a complex drug manufacturing extension project.
CQV Engineer Responsibilities:
- Participates in construction walkdowns.
- Part of the CQV Team in relation to punch list closure during M/C and during the CQV execution phase.
- Lock Out / Tag Out. (LOTO)
- Ensure compliance with all local codes and regulations, including ATEX directives.
- Reviews and approves commissioning protocols associated with area of expertise.
- Supports team on troubleshooting during start-up/commissioning activities.
- Liaise with CQV and Lead Scheduler in relation to management for all Electrical Systems, ensuring all correct predecessors and successors are in place.
- Liaises with other disciplines to ensure alignment and coordination across disciplines.
- Liaise with all Project Groups (CM/CQV/Automation/Process/SMEs/Ops/Maintenance/PMs) to ensure all Electrical Systems are managed appropriately for the entire Project Lifecycle.
- Ensure proper installation details and studies are developed and that it is protected at the soonest opportunity following installation.
- Partner with CM to ensure quality of installation follows requirements and expectations.
- Coordinate with CM and system owners during walk downs and agree the categorisation of punch items.
About you:
- Degree in Electrical Engineering or Equivalent qualification/Experience.
- Minimum of 5 years’ experience in a similar regulated industry including experience with construction commissioning, Qualification & Validation.
- Punch lists, Walk downs, LOTO.
- An understanding of all applicable electrical engineering codes, standards and acceptable industry standards.
- Experience with complex projects and working in or around operating facilities.
- Experience in troubleshooting and providing support for Electrical Systems in a GMP Environment.
- Demonstrated proficiency communicating and collaborating at a variety of levels with customers, vendors, equipment suppliers and operations staff.
Are you a good fit for a CQV Engineer? Get in touch with us today.
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
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
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
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