CSV Engineer
- Denmark
- Contract
- CAPEX Projects
This vacancy has now expired
Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CSV 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.
Responsibilities:
- Generate any needed automation Validation Plans.
- Generate and execute Automation Commissioning and Qualification test protocols for the Automation systems in scope of the project (e.g., DeltaV, Syncade, PI, Infobatch)
- Support and participate in system testing
- Clarify discrepancies and review/approve executed test protocols
- Secure right quality strategy related to requirement and design documents and quality activities.
- Comment/challenge and coordinate review of design documentation.
- Support design quality activities in relation to automation.
- Support the automation team in test execution and final report writing.
Requirements:
- 5+ years’ experience as CSV engineer working with automation in large pharma / biotech projects.
- Experience with Automated systems, such as Delta V / Syncade / PI / Infobatch
- Solid process understanding combined with automation understanding
- Experience from the pharmaceutical or biotechnology industry.
- Knowledge of batch processes, GMP, GAMP and the S88 standard.
If this role is of interest to you, please apply now!
#LI-ML1
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
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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