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Supplier Quality
- Contract
- Good Manufacturing Practice (GMP)
- Switzerland
This vacancy has now expired. Please see similar roles below...
Proclinical are recruiting for a Supplier Quality to join a biotech organisation. This role is on a contract basis with the ability to work remotely in Switzerland.
Responsibilities:
- Handle allocated systems and tools in an optimised way to enable lean international actions of QAA's.
- Work alongside management and peers to report on progress for tight timelines of QAA remediation project.
- To handle end-to-end QAA establishment process from writing to signatures and suitable system upload, you will be responsible for supplier lifecycle management for project international QAA remediation.
- Uphold data integrity and guarantee compliance with company SOPs and specifications, FDA, and cGMP guidelines.
- Other duties may be assigned to this role.
Key Skills and Requirements:
- Educated to a degree level.
- Expertise on cGMPs and cGDP needs, ISO standards for supplier qualification and QAA establishment process.
- Familiarity with both supplier qualification and supplier supervision.
- Works well independently with the ability to take risk-based decisions.
- Solid deliberations abilities.
- Fluency in the English language.
- Communication skill both verbally and in writing.
If you are having difficulty in applying or if you have any questions, please contact Will Hitchcock at +44 203 0789 554.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.
Proclinical Staffing is an equal opportunity employer.
#QACompliance
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