DePuy Synthes, the worldwide leader in the development of products to treat orthopaedic trauma and other bone deformities headquartered in West Chester and Solothurn, Switzerland and employing over 1,000 people worldwide, has the following Chester County career positions posted on their career page:

Worldwide Product Director

DePuy Synthes seeks a Worldwide Product Director in their Synthes Trauma business unit, the worldwide leader in the development of products to treat orthopaedic trauma and other bone deformities. This position is responsible for the worldwide marketing of products within one of the company’s anatomic business units (Hip & Pelvis, Knee, Platform Technologies, Hand & Wrist, Shoulder & Elbow, or Foot & Ankle). Various functions of the Worldwide Product Director include driving commercial results, developing brand strategies, identifying customer insights, developing and executing business plans, portfolio management, product development, product launches and general business support.

The Worldwide Product Director candidate should have a Bachelor’s or an MBA degree and a minimum of 5 years progressive business experience in any of the following areas: Marketing, Medical Device Product Development R&D, Medical Device Sales, or a combination of sales and marketing. The successful candidate should have experience developing and executing successful business plans and managing medical device product lines, including leading product development teams and setting strategic direction for a product portfolio is preferred. Fluency in Swiss-German or German is preferred.

Click here for more information on the Worldwide Product Director career position at DePuy Synthes or to apply online.

Senior Quality Engineer

DePuy Synthes seeks a Senior Quality Engineer to lead improvement and remediation projects for the company’s global field action department. Additionally, the position will be responsible for conducting field action investigations for patient safety, including managing Preliminary Risk Assessment, Health Hazard Evaluation and Quality Review Board meetings. This position will be coordinating the projects and investigation activities with Subject Matter Experts from risk management, medical, design, manufacturing, and distribution, ensuring accuracy and robustness of information received, preparing documentation and presenting issues to management level review boards.

The ideal candidate for the Senior position will have a Bachelor’s or advanced degree in Engineering or Technical Science and a minimum of 4 years of experience in a medical device or pharma industry. Previous involvement with Patient Safety and field action activities is preferred as is a working knowledge of 21 CFR Part 820, QSR, ISO 13485, and MDD/IVDD requirements and strong computer (e.g., PowerPoint, WORD, Excel, Visio), communication, and written skills are required.

Click here for more information on the Senior Quality Engineer career position at DePuy Synthes or to apply online.

Regulatory Specialist

The Regulatory Specialist will be responsible for supporting field action execution activities including attending Field Action Strategy Team meetings, support the preparation of document packages to notify regulatory agencies of field action activities, providing updates to FDA and global regulatory agencies, processing and closing Field Actions in a timely manner, and act as support for FDA and regulatory inspections.

The Regulatory Specialist candidate should have a Bachelor’s Degree in engineering or technical and a minimum of 2 years of experience in a GMP or ISO regulated industry is required, medical device and/or pharmaceutical industry preferred and one or more years of experience within a regulatory role. Experience with field action related activities and with health authority interactions is preferred.

Click here for more information on the Regulatory Specialist career position at DePuy Synthes or to apply online.