QAV Specialist
- Poland
- Contract
- Commissioning, Qualification and Validation
This vacancy has now expired
Our client, a leading biologics manufacturing organisation, are searching for a QAV Specialist to join them on their newest expansion project. With a significant investment underway, they are currently looking for support with the expansion of their QC Labs and manufacturing lines.
This is an initial 6-month contract with likely extensions.
QAV Specialist Responsibilities:
- Production and QC equipment validation documentation review and approval
- Critical utilities validation documentation review and approval.
- Validation SOPs review and approval
- Deviation related to validation studies review and approval
- 3-8 years’ experience within a GMP environment
- Experience reviewing validation documentation for:
- QC Lab equipment,
- HVAC,
- water system,
- gas systems,
- clean steam
- Review and approval of deviation studies
The candidate must have the rights to work in the location stated in the job advert.
Please note, Quanta part of QCS Staffing does not sponsor Visa applications.
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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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