QAV Specialist
- Denmark
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a QAV Specialist 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.
Responsibilities:
- Create, approve and maintain quality plans and procedures.
- Review and approve SAT/IQ/OQ and PQ for major process equipment being the isolator base filling line
- QA involvement in clean room area readiness and qualification
- Involvement in internal Mock-up audits to prepare for GMP inspection.
- Minimum 5 years QAV Biotech experience on Large Scale Projects
- SME on all Quality and Compliance issues - minimum 5 years
- Working knowledge of ASTM E2500 / Leveraging Verification process
- Experience with design and construction projects for manufacturing facilities.
- Experience with complex projects and working in or around operating facilities.
- Ability to keep work pace and meet deadlines.
- Good organising and planning skills.
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
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
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