Set up as a new job alert
Set up as a new job alert
Enter your email below to receive alerts to your inbox when similar jobs become available.
By clicking "Yes, send me jobs" below you are consenting to receive jobs to your inbox, based on the search criteria you have selected, as per our privacy policy.
By clicking "Yes, send me jobs" below you are consenting to receive jobs to your inbox, based on the search criteria you have selected, as per our privacy policy.
Thank you for signing up for a Job Alert
15968en
- Contract
- English
- Associate
- Engineering & Technical Services
- Neuchâtel
- Healthcare & Life Sciences
Skills
CQV, Engineer, Process Engineer, Qualification activities, GMP
Click here to get a notification every time a job like this gets added
Great news! We will let you know when a new job like this has been added!
This vacancy has now expired
Start Date: As soon as possible
Location: Neuchatel
Workload: 100%
Work type: Hybrid
Duration: 2 months’ (extension possible)
Your mission:
Our client is currently executing a capacity extension Project.
The project is in its final stages (CQV-End of SAT, PQ) and require support for the remaining engineering activities.
You will support the current Engineering activities on the project, specifically (but not only) on:
- Sink sanitization:
-Perform commissioning and Qualification activities (static and dynamic SAT) as Executor/review/Approver accordingly to the need in accord with the cGMP and client’s execution standards.
- Heating Loop Z481:
-Represent the client F&U Qualification requirement with Supplier or third Part.
-Perform revision of all technical documentation (P&ID, Technical specification, Spare List,).
-SAT protocols writing (static, automation, dynamic.
-Perform Commissioning and Qualification activities as executor/reviewer/approver accordingly to the need in accord with the cGMP and the client’s execution standards.
- Perform the coordination of suppliers’ intervention according to the Neuchâtel Site.
- Technical oversight and support as required for activities being carried out on the project.
- Provide process/FU support for engineering, qualification, and validation of new equipment.
- Provide ongoing technical support for change control, deviation investigations and CAPA management.
Your background:
- Experience with CQV activities and the work tasks mentioned above.
- Available as soon as possible.
What’s an offer?
- Chances to grow within a leading pharmaceutical company.
- Hybrid work model.
- Dynamic work environment.
Location: Neuchatel
Workload: 100%
Work type: Hybrid
Duration: 2 months’ (extension possible)
Your mission:
Our client is currently executing a capacity extension Project.
The project is in its final stages (CQV-End of SAT, PQ) and require support for the remaining engineering activities.
You will support the current Engineering activities on the project, specifically (but not only) on:
- Sink sanitization:
-Perform commissioning and Qualification activities (static and dynamic SAT) as Executor/review/Approver accordingly to the need in accord with the cGMP and client’s execution standards.
- Heating Loop Z481:
-Represent the client F&U Qualification requirement with Supplier or third Part.
-Perform revision of all technical documentation (P&ID, Technical specification, Spare List,).
-SAT protocols writing (static, automation, dynamic.
-Perform Commissioning and Qualification activities as executor/reviewer/approver accordingly to the need in accord with the cGMP and the client’s execution standards.
- Perform the coordination of suppliers’ intervention according to the Neuchâtel Site.
- Technical oversight and support as required for activities being carried out on the project.
- Provide process/FU support for engineering, qualification, and validation of new equipment.
- Provide ongoing technical support for change control, deviation investigations and CAPA management.
Your background:
- Experience with CQV activities and the work tasks mentioned above.
- Available as soon as possible.
What’s an offer?
- Chances to grow within a leading pharmaceutical company.
- Hybrid work model.
- Dynamic work environment.
I manage this role