Design Quality Engineer Job

Job description

Design Quality Engineer-000011K1Description"Caring for the world… one person at a time” inspires and unites the people of Johnson & Johnson. This culture of caring is the focus of our corporate philosophy, that are anchored in the internationally applicable CredoDePuy Synthes Companies of Johnson & Johnson is the largest, most comprehensive orthopedic and neurological business in the world. DePuy Synthes offer an unparalleled breadth and depth of technology, devices, services and programs in the areas of joint reconstruction, trauma, spine, sports medicine, neurological, cranio-maxillofacial, power tools and biomaterials. Our broad array of inspired, innovative and high-quality offerings help advance the health and wellbeing of people around the world.
For our Headquarters in Zuchwil, Solothurn we are looking for a highly committed Design Quality EngineerWorking in the Design Quality team the qualified candidate for this hands-on position should excel in an environment that embraces teamwork, change, risk-based decision making and flexibility. This individual should be willing to make a significant contribution to a multi-discipline team, must be self-motivated to take action, and have excellent written and verbal communication skills. This position will also hold responsibility for Lifecycle Management and Base Business support to ensure the highest levels of product quality to the end customer.
Your responsibilities
- Design Quality team member focused on life cycle management activities.
- Execute the Design Control and Risk Management processes to better reflect state of the art practices and drive continuous improvement.
- Support design control activities for product improvement efforts for existing products.
- 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, Post Market Surveillance, Nonconforming Materials, Risk Management, etc.
- 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 to maintain the highest levels of professionalism, ethics and compliance at all times.
Qualifications
- A minimum of a Bachelor's degree in Engineering or related technical or scientific discipline with a minimum of 4+ years of experience is required. A Master’s degree in a technical discipline is an asset.
- Excellent problem solving and decision-making skills are required.
- Interpersonal skills that foster conflict resolution are required.
- Experience with Blueprint reading/literacy including GD&T is preferred.
- Previous Quality Engineering experience is preferred.
- Previous experience in a medical device or a healthcare discipline is preferred.
- Working knowledge of Design Controls, GMPs, QSR, 21 CFR 820, MDD 93/42/EEC, ISO13485 and ISO14971 quality requirements is preferred.
- Experience conducting Process / Design Failure Mode and Effects Analysis is preferred.
- Working knowledge of material science and mechanical product knowledge is preferred.
- Fluency in English is required, good knowledge of German would be a strong asset.
If you feel attracted by this challenge and want to be part of a successful and growing organization, then please send us your online application (CV, Motivation Letter, Working References etc.).Primary Location:Europe/Middle East/Africa-Switzerland-Solothurn-ZuchwilOrganization: Synthes GmbH (7111)Job Function: Quality