CQV Stream Manufacturing
- France
- Contract
- CAPEX Projects
Our client is a renowned European consulting firm specialising in the life sciences industry. With a strong focus on quality, regulatory compliance, and project management, our client provides comprehensive solutions to help clients navigate the complex landscape of drug development, medical device manufacturing, and healthcare services.
Profile sought:
- 5 to 10 years experience in qualifying UpStream and DownStream manufacturing equipment
- Experience in execution on equipment such as: Bioreactor, skid, Low Flow Chromatography skid, TCU Purification, Autoclave, Bag integrity tester, Centrifuge,
- Mastery of writing non-compliance management.
- Knowledge of Delta V is a plus
- Autonomous, flexible, collaborative Role: You will join the manufacturing equipment qualification execution team on our client's site located in Toulouse.
- Execute manufacturing equipment qualification protocols
- Manage qualification non-conformities (investigation, assessment, CAPA proposal)
If this role is of interest to you, please apply now!
#LI-CO1
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
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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Caroline
I manage this role.