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Supplier Quality Engineer Contract (m/w/d) (DE)

[13321]
Medizintechnik, Supplier Quality Engineer (SQE) , ISO 13485

Job title: Supplier Quality Engineer Contract (m/w/d) Industry: Medizintechnik Skills: Medizintechnik, Supplier Quality Engineer (SQE) , ISO 13485 Start of project: ASAP Duration of the project : 6 Months Project volume: 1008 Hours  Location: Zürich, Schweiz Tasks: ·Ensure the implementation, monitoring and effective completion of the supplier quality management in accordance with the quality management strategy and requirements. ·Collaborate closely with Engineering, operations and purchasing to assess, select and qualify new suppliers and to qualify critical components. ·Initiate, lead and conclude Quality Agreements with suppliers. Skills: ·Proven experience in performing supplier audits ·Strong experience in quality assurance for products (class I, lla/llb). ·Knowledge and working experience of quality management ·system, standards and government regulations applicable to medical devices e.g. ISO 13485, 21 CFR 820 QSR, MDSAP, MDD 93/42/EEC and (EU) 2017/745 (MDR). ·5+ years of work experience in the Medical Device Business (QARA), with cross-functional experience in international environment.

Job title: Supplier Quality Engineer Contract (m/w/d)
Industry: Medizintechnik
Skills: Medizintechnik, Supplier Quality Engineer (SQE) , ISO 13485
Start of project: ASAP
Duration of the project : 6 Months
Project volume: 1008 Hours 
Location: Zürich, Schweiz

Tasks:
  • Ensure the implementation, monitoring and effective completion of the supplier quality management in accordance with the quality management strategy and requirements.
  • Collaborate closely with Engineering, operations and purchasing to assess, select and qualify new suppliers and to qualify critical components.
  • Initiate, lead and conclude Quality Agreements with suppliers.

Skills:
  • Proven experience in performing supplier audits
  • Strong experience in quality assurance for products (class I, lla/llb).
  • Knowledge and working experience of quality management
  • system, standards and government regulations applicable to medical devices e.g. ISO 13485, 21 CFR 820 QSR, MDSAP, MDD 93/42/EEC and (EU) 2017/745 (MDR).
  • 5+ years of work experience in the Medical Device Business (QARA), with cross-functional experience in international environment.

map Zürich, Schweiz date_range ASAP update Temporary
Direct contact

Minette Potger

Recruitment Consultant
mail m.potger@aristo-group.ch
phone +41 44 274 39 00


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