Design Quality Engineer - Orthopaedic Medical Devices

Vertragsart:
Vor Ort
Start:
01/10/2018
Dauer:
01/10/2019
Von:
Michael Bailey Associates - Munich
Ort:
Solothurn
Eingestellt:
10.08.2018
Land:
flag_no Schweiz

Projektbeschreibung
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For our Medical Device client we are recruiting for a Design Quality Engineer who will assist in the design and quality efforts with Orthopaedics. This is a contract position for 1 year.

Requirements:

  • 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.

Responsibilities:

  • A minimum of a Bachelor's degree in Engineering or related technical or scientific discipline with a minimum of 7+ 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.
  • Experience in an Medical Device regulated environment
  • 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.
  • Excellent problem solving, decision-making, and root cause analysis skills are required.
  • Interpersonal skills that foster conflict resolution are required.
  • Ability to multi-task independently with minimal supervision
  • Working knowledge of material science and mechanical product knowledge
  • Development and manufacturing experience is preferred.

Please send CVs or call

Michael Bailey International is acting as an Employment Business in relation to this vacancy.