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Quality Engineer (m/f)
Eingestellt von Stamford Consultants AG
Gesuchte Skills: Engineer, Support
Projektbeschreibung
Our client, international biopharmaceutical company based in Basel area, is currently looking for a Quality Engineer (contract).
Important: For this role a valid Swiss working/residency permit or EU citizenship is required.
MAIN RESPONSIBILITIES:
- Ensuring and verifying product quality
- Assigned products technical release
- Processing quality notifications (OP) and technical review for deviations including documentation
- Troubleshooting and technical support in within QC area
- Analysis and trending of quality data
- Analysis RFT data
- Continuous optimization of the workflow for quality and efficiency improvement
- Manufacturing and testing processes
- Support Product Leaders and Head of Department in cost reduction, CAPA implementations, ICM tasks
- Coordination between QA, R&D, QC and production line
- Create, update relevant documents and reports
IDEAL PROFILE:
- Experience as Project-/Quality Engineer, or similar within quality assurance
- Laboratory experience is an advantage
- Experience in the highly regulated GxP environment of MedTech, ISO 13458, GMP, FDA 21 CFR
- Fluency in English, German is advantageous
If you will be interested in this or other contacting positions please send your CV
Important: For this role a valid Swiss working/residency permit or EU citizenship is required.
MAIN RESPONSIBILITIES:
- Ensuring and verifying product quality
- Assigned products technical release
- Processing quality notifications (OP) and technical review for deviations including documentation
- Troubleshooting and technical support in within QC area
- Analysis and trending of quality data
- Analysis RFT data
- Continuous optimization of the workflow for quality and efficiency improvement
- Manufacturing and testing processes
- Support Product Leaders and Head of Department in cost reduction, CAPA implementations, ICM tasks
- Coordination between QA, R&D, QC and production line
- Create, update relevant documents and reports
IDEAL PROFILE:
- Experience as Project-/Quality Engineer, or similar within quality assurance
- Laboratory experience is an advantage
- Experience in the highly regulated GxP environment of MedTech, ISO 13458, GMP, FDA 21 CFR
- Fluency in English, German is advantageous
If you will be interested in this or other contacting positions please send your CV
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges