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Supplier Quality Engineer
Eingestellt von Larson Group
Gesuchte Skills: Support, Engineer
Projektbeschreibung
REFERENCE: JNJ
ROLE: Supplier Quality Engineer
SKILLS: Quality Approval for New Suppliers/Manage Supplier products
LOCATION: Zuchwil, Switzerland
HOURS: Hours per Day 8, Hours per Week 40, Total Hours 1424
EXTRA: English and Swiss German spoken and written
SUPPLIER QUALITY ENGINEER:
Main focus on QUALITY AGREEMENTS (creation, negotiation)
Contract Management skills is a must
General Job Description:
- Implement SQ strategy and follow Supplier Quality standards
- Manage supplier related Non-Conformities (NC's)
- Manage supplier related Corrective and Preventive Actions (CAPA's)
- Manage supplier change requests
- Responsible for Process Validations at supplier and to maintain a validation master plan
- Manage supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)
- Perfom product investigations
- Support supplier preparation for FDA inspections
- Supplier transfer projects
- Support for supplier selection
- Support for Quality Agreement
Specific:
- Part of Global Remediation Quality Plan Project (GRQP)
- ASL Legacy remediation: creation of Quality/Change agreements, Desktop audits
- Master data Management
- Quality approval for new suppliers according to procedure
- Non-Technical profile requirements:
- Some flexibility in working hours is required
- Must be able to work on multiple simultaneous tasks with limited supervision;
- Language proficiencies: -English and Swiss German spoken and written
ROLE: Supplier Quality Engineer
SKILLS: Quality Approval for New Suppliers/Manage Supplier products
LOCATION: Zuchwil, Switzerland
HOURS: Hours per Day 8, Hours per Week 40, Total Hours 1424
EXTRA: English and Swiss German spoken and written
SUPPLIER QUALITY ENGINEER:
Main focus on QUALITY AGREEMENTS (creation, negotiation)
Contract Management skills is a must
General Job Description:
- Implement SQ strategy and follow Supplier Quality standards
- Manage supplier related Non-Conformities (NC's)
- Manage supplier related Corrective and Preventive Actions (CAPA's)
- Manage supplier change requests
- Responsible for Process Validations at supplier and to maintain a validation master plan
- Manage supplier product PVE's (First Article Inspection, Control Plans, Critical to Quality, Capability studies)
- Perfom product investigations
- Support supplier preparation for FDA inspections
- Supplier transfer projects
- Support for supplier selection
- Support for Quality Agreement
Specific:
- Part of Global Remediation Quality Plan Project (GRQP)
- ASL Legacy remediation: creation of Quality/Change agreements, Desktop audits
- Master data Management
- Quality approval for new suppliers according to procedure
- Non-Technical profile requirements:
- Some flexibility in working hours is required
- Must be able to work on multiple simultaneous tasks with limited supervision;
- Language proficiencies: -English and Swiss German spoken and written
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik, Sonstiges