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Design Quality Engineer

  • Salaire: CHF75 - CHF83 per hour
  • Type d'emploi: Contract, Full-time
  • Lieu: Oberdorf
  • Secteur: Other, Pharma & Life Sciences
  • Date de mise en ligne: 19/09/2018
  • Référence du poste: BBBH87695
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Design Quality Engineer

Experis IT is Europe's leading IT recruitment agency. We are dedicated to connecting talented individuals with Business opportunities across a number of professional sectors, with IT being at the heart of our operations.

For one of our client, specialized in the medical devices area based in Oberdorf we are looking for a Design Quality Engineer.

This is a challenging, contracting position, starting November until the end of March 2019.

Responsibilities:

  • Design Quality team member focused on life cycle management activities
  • Enhance the Design Control and Risk Management processes to better reflect state of the art practices and drive continuous improvement.
  • Apply statistical methods and process/design excellence tools to establish test plans as well as evaluate test data and processes. Perform Gage R&R studies.
  • Conduct and lead design verification and validation activities.
  • Conduct and lead design / process failure mode effects and analysis.
  • Provide leadership in all areas of the Quality System, including, but not limited to Corrective & Preventive Actions, Complaints, Nonconforming Materials, Risk Management, etc.
  • Provide leadership in the understanding of medical device regulations to other disciplines.
  • Communicate effectively at all levels within Quality as well as cross functionally with departments such as Product Development, Regulatory Affairs, Manufacturing, and Marketing.
  • Know and follow all laws and policies that apply to the job, and maintain the highest levels of professionalism, ethics and compliance at all times.
  • Accountable for the successful delivery of multiple simultaneous projects, spanning multiple functional areas and locations.
  • Responsible of clear definition of project scope and deliverables, milestones and timeline, project risks and contingency plans.
  • Additional duties as assigned.

You bring to this role:

  • Bachelor's degree in Engineering or related technical or scientific discipline with a minimum of 5 years of experience in related field is required.
  • Proven exceptional written and oral presentation skills
  • Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485 and ISO14971 quality requirements is required
  • Previous Quality Engineering
  • Experience in an Medical Device regulated environment
  • Strong knowledge and skills in MS Office
  • Strong quality engineering skills with a proven track record in design verification/validation, process verification/validation, and design/process Failure Mode and Effects Analysis is preferred.
  • Ability to multi-task independently with minimal supervision
  • Working knowledge of material science and mechanical product knowledge is preferred.
  • Development and manufacturing experience is preferred.
  • Fluency in English is required; good knowledge of German would be a strong asset.

Start Date: 01/11/2018

Location: Oberdorf

If you've any further questions on the role, please call Julie Mackerer on +41 61 282 22 17.

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