QA Review Specialist
- Denmark
- Contract
- CAPEX Projects
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a QA Review 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:
- Review and approval of PQ protocols and reports
- Review and approval of PQ related deviation
- QA oversight activities
- Look at deviations and changes cases
- he entire review and validation process
Requirements:
- Min. 5-10 years of QA experience
- Previous experience of review and approval of PQ protocols
- Previous experience of managing deviations and change controls
- Pharma experience
- Adaptable in an ever-changing project environment
If this role is of interest to you, please apply now!
#LI-HS1
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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