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Supplier Quality Engineer

Eingestellt von Michael Bailey Associates - Munich

Gesuchte Skills: Engineer, Support

Projektbeschreibung

SUPPLIER QUALITY ENGINEER

Zurich Area/Switzerland

Global Medical Device Company

6 Month Contract

JOB SUMMARY

The Supplier Quality Engineer (SQE) will support the Supplier Quality Management. This position must drive incoming quality by evaluating new and existing suppliers, driving the incoming quality verification program at the company, and resolving supplier issues to closure in a timely manner.

SQE will provide supplier qualifications, material and manufacturing issue resolution, driving supplier corrective actions, and maintain the approved supplier list.

Furthermore the SQE contributes to optimize added value and business success by maintaining, reviewing, operating and further developing process oriented organizational system (incl. suppliers). To execute supplier audits per compliance with regulatory and corporate requirements is a job requirement as well.

PROFESSIONAL SKILLS

Approve supplier selection through robust qualification processes

Carrying out external system and process audits at international suppliers as a lead auditor

Developing, negotiating and concluding Quality Assurance Agreements with subcontractors

Following-up of supplier Corrective Actions and reporting related indicators

Assisting project teams within the organization on quality related issues

Manages and monitors implementation and effectiveness of corrective actions related to Non-conformance findings

Assists suppliers in developing strategies for corrective action and preventive action

Develops indicators and data for tracking and trending of supplier quality

Develops positive relationships and works closely with Global Supplier Management to manage and implement supplier changes, New Product introductions, and transfer projects.

EDUCATION

Position requires a sound technical background (University degree, technical degree or equivalent)

Quality Manager training with Diploma certificate (ie SAQ or equivalent) and Auditor training with Diploma certificate (ie SAQ or equivalent) required

Experience in manufacturing industry (preferably Medical Device or Pharma) and in Quality organization, Lead Auditor experience

Broad knowledge of Regulatory requirements (ISO 13485/21 CFR 820/cGMP/MDD, etc.)

Experience in interpreting and applying regulations and standards, auditing to these and possesses good oral and written communications skills

Good problem-solving ability and analytical skills, strong sense of initiative and attention to detail

Excellent interpersonal skills

Excellent oral and written communications abilities in German and English. Other languages beneficial.

Familiar with a variety of Office Software packages including MS Word, Powerpoint, Visio, Excel, SAP and MS Project, etc.Michael Bailey International is acting as an Employment Business in relation to this vacancy.

Projektdetails

  • Einsatzort:

    Zürich, Schweiz

  • Projektbeginn:

    asap

  • Projektdauer:

    6months

  • Vertragsart:

    Contract

  • Berufserfahrung:

    Keine Angabe

Geforderte Qualifikationen

Michael Bailey Associates - Munich