Senior Quality Assurance Specialist (f/m/d)
at Lonza
Visp, VS, Switzerland -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 09 Feb, 2025 | Not Specified | 10 Nov, 2024 | N/A | Life Science,Biotechnology | No | No |
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Description:
Today, Lonza is a global leader in life sciences operating across three continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
In Visp, we are looking for a QA Specialist (f/m/d) to extend our team. You will report to the QA Operations Team lead Microbial and work in close collaboration with different quality and operations functions in order to ensure cGMP-compliant manufacturing activities and documentation.
Key responsibilities:
Responsibilities:
- Responsible in full for adherence with the quality agreement provisions
- Responsible to ensure all deviations are appropriately investigated and recorded.
- Responsible to drive CAPA items to complete and timely completion
- Directs the investigations of customer product complaints and assures the completion of the appropriate documentation
- Performs assessments for all product-related changes, assess relevance to regulatory filings, decide to implement and provide change controls for approval to customers where required
- Ensures an efficient cGMP compliant life cycle management of all products manufactured
- Has the authority to make quality decisions for the project in internal and external meetings
REQUIREMENT SUMMARY
Min:N/AMax:5.0 year(s)
Pharmaceuticals
Pharma / Biotech / Healthcare / Medical / R&D
Software Testing, Clinical Pharmacy
MSc
Life science (e.g
Proficient
1
Visp, VS, Switzerland