embecta is one of the largest pure-play diabetes care companies in the world, leveraging its nearly 100-year legacy in insulin delivery to empower people with diabetes to live their best life through innovative solutions, partnerships and the passion of approximately 2,000 employees around the globe. For more information, visit  embecta.com  or follow our social channels on  LinkedIn ,  Facebook ,  Instagram  and  Twitter .

embecta is looking for an experienced Staff Manufacturing Engineer to join our team. This technical expert will play a critical role in executing the manufacturing strategy, implementing new processes, conducting process improvement, and delivering manufacturing advancement projects. The ideal candidate will have a proven track record of excellence and passion for developing new products/processes within the medical device industry. A key element of this experience is in managing cross-functional manufacturing engineering projects and inspiring collaboration throughout the organization.

The Staff Manufacturing Engineer, New Product Development (NPD), will function as an individual contributor and subject matter expert; leading the development and implementation of manufacturing process technologies to realize products in the embecta infusion platform. This talented and passionate individual will be responsible for delivering innovative and practical manufacturing solutions that support a product development road map aimed at realizing the commercialization of a complicated electro-mechanical device. Focus for this role will be on manufacturing process development, leading design of manufacturing methods and fixtures, establishing lean manufacturing cells, and coordination of the test method development as a liaison for design transfer. The Staff Manufacturing Engineer, NPD will deliver DFM analysis, develop manufacturing process specifications, support first-of-type semi and fully automated manufacturing equipment, and transition processes into production.

Key Elements of this Role Include:

• Responsible for design and characterization of prototype equipment and pilot processes in support of manufacturing scale-up and launch.

• Manage internal and external resources, in the development of manual and semi-automated processes for product assembly.

• Oversees the development of production and process control documents, prepares technical analysis, recommends manufacturing methods and processes required to meet design objectives on new or improved products and/or processes.

• Apply lean manufacturing methodologies to characterize, debug, and optimize manufacturing processes.

• Support Design for Manufacturing/Assembly (DFM/A) activities and process specification definition throughout product development lifecycle.

• Support root cause investigations and manufacturing process improvements.

• Support/perform design reviews, FMEA’s, risk / hazard analysis & establishing technical requirements.

• Support identification and qualification of suppliers for specialty materials, finished goods, and equipment.

• Support 3D modeling and tolerance analysis of complex electro-mechanical systems.

• Works with globally located and cross functional teams at business unit and plant level to achieve project goals.

• 10 – 25% travel

Requirements:

Education: B.S. degree in Mechanical, Biomedical, or related Engineering discipline is required. Masters' degree or MBA preferred.

Experience: 5+ years relevant experience, in the fields of process and project engineering supporting new product development and delivering new manufacturing processes within the medical device industry. Experience with electro-mechanical devices preferred.

embecta is an Equal Opportunity/Affirmative Action Employer. We do not unlawfully discriminate on the basis of race, color, religion, age, sex, creed, national origin, ancestry, citizenship status, marital or domestic or civil union status, familial status, affectional or sexual orientation, gender identity or expression, genetics, disability, military eligibility or veteran status, or any other protected status.