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Archiviertes Projekt - Design Quality Engineer JNJKJP00034640 (m/f) 395305/29

Januar 2019

Dezember 2019

CH-Solothurn

nicht angegeben

10.01.2019

395305/29

Projektbeschreibung

Ihre Aufgaben:
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

Ihre Qualifikationen:
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
Excellent problem solving, decision-making, and root cause analysis skills are required
Interpersonal skills that foster conflict resolution are required
Experience in an Medical Device regulated environment
Fluency in English is required, good knowledge of German would be a strong asset
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
Previous Quality Engineering experience is preferred


Projektstart: asap
Projektdauer: 11 MM++


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