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Quality Engineer - Medical Devices
Eingestellt von Sentinel IT LLP
Gesuchte Skills: Engineer, Engineering
Projektbeschreibung
Quality Engineer - Medical Devices
Leading global Pharmaceutical, require a Quality Engineer for a long-term contract with their Medical Device subsidiary - working with suppliers on product transfer projects.
General Job Description:
- Manage product transfer projects.
- Train/coach suppliers on process engineering
- Manage Supplier Process Verification:
- Creation/review of Process Flow Plan
- Creation/review of Process Risk Assessment (FMEA)
- Creation/review of Process control plans
- Creation/review of Measurement Systems Evaluation
- Creation/review of special process validation
- Creation/review of manufacturing material lists
- Creation/review of first article inspections
- Creation/review of capability studies
- Creation/review of environmental test
Potentially additional tasks:
- Manage supplier related Non-Conformities (NC's)
- Manage supplier related Corrective and Preventive Actions (CAPA's)
- Manage supplier change requests
Non Technical Skills and Additional Details
Non-Technical profile requirements:
- Good communicator with leadership skills
- Adequate appearance to be able to visit/coach suppliers
- Some flexibility in working hours is required
- Must be able to work on multiple simultaneous tasks with limited supervision
- Quick learner, motivated self-starter; - Excellent customer service, interpersonal, communication and team collaboration skills
- Able to follow change management for internal guidelines.
Language proficiencies: -English and German spoken and written
Please apply now for more details!
Leading global Pharmaceutical, require a Quality Engineer for a long-term contract with their Medical Device subsidiary - working with suppliers on product transfer projects.
General Job Description:
- Manage product transfer projects.
- Train/coach suppliers on process engineering
- Manage Supplier Process Verification:
- Creation/review of Process Flow Plan
- Creation/review of Process Risk Assessment (FMEA)
- Creation/review of Process control plans
- Creation/review of Measurement Systems Evaluation
- Creation/review of special process validation
- Creation/review of manufacturing material lists
- Creation/review of first article inspections
- Creation/review of capability studies
- Creation/review of environmental test
Potentially additional tasks:
- Manage supplier related Non-Conformities (NC's)
- Manage supplier related Corrective and Preventive Actions (CAPA's)
- Manage supplier change requests
Non Technical Skills and Additional Details
Non-Technical profile requirements:
- Good communicator with leadership skills
- Adequate appearance to be able to visit/coach suppliers
- Some flexibility in working hours is required
- Must be able to work on multiple simultaneous tasks with limited supervision
- Quick learner, motivated self-starter; - Excellent customer service, interpersonal, communication and team collaboration skills
- Able to follow change management for internal guidelines.
Language proficiencies: -English and German spoken and written
Please apply now for more details!
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Ingenieurwesen/Technik