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Project Engineer responsible for leading product development programs from quoting through production launch within medical device and plastics manufacturing environments. Job Requirements Bachelor's degree in Mechanical Engineering, Plastics Engineering, or related engineering discipline. 5+ years of project engineering experience. 5+ years of plastics manufacturing experience. 5+ years of plastics injection molding experience. Experience reviewing part designs for draft, side actions, shutoffs, and manufacturability. Knowledge of plastic mold features driven by part geometry. Knowledge of plastic mold construction and mold design review. Experience with medical molding. Experience with High-Consistency Rubber, gum silicone, and/or Liquid Silicone Rubber molding. Knowledge of Advanced Product Quality Planning (APQP). Experience with Design of Experiments (DOE). Experience performing capability studies. Knowledge of steel-safe and tolerance-safe tooling concepts. Experience managing project timelines using tools such as Microsoft Project and Gantt charts. Experience managing multiple suppliers, including mold makers and material suppliers. Experience managing project budgets. Proficiency with Microsoft Excel and Word. Experience using ERP systems; IQMS experience preferred. Preferred Skills 5+ years of experience in the medical device industry. Experience with thermoplastic injection molding. Experience with thermoset injection molding. Experience with automation systems including press robots and automated assembly equipment. Experience with secondary operations including deflashing, assembly, testing, and decorating. Experience evaluating manufacturing options based on cost impact. Experience supporting medical device component manufacturing programs. Job Responsibilities Lead cross-functional engineering programs from quoting through production launch. Review product designs for manufacturability and tooling requirements. Evaluate mold designs, tooling concepts, and mold construction approaches. Support development of medical molding processes and production methods. Apply APQP methods throughout product and process development. Develop and support DOE activities and capability studies. Evaluate tooling strategies using steel-safe and tolerance-safe concepts. Coordinate automation requirements, including press robots and automated assembly equipment. Develop and evaluate secondary manufacturing operations. Compare manufacturing and tooling options based on technical requirements and cost impact. Develop and maintain project schedules, milestones, and Gantt charts. Coordinate activities with mold makers, material suppliers, and other external suppliers. Track project budgets, tooling costs, and manufacturing development expenses. Support production readiness and manufacturing launch activities. Maintain project, tooling, process, and production documentation within ERP and business systems.

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The Company will consider qualified applicants with arrest and conviction records in accordance with federal, state, and local laws and/or security clearance requirements, including, as applicable: The California Fair Chance Act Los Angeles City Fair Chance Ordinance Los Angeles County Fair Chance Ordinance for

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It is unlawful in Massachusetts to require or administer a lie detector test as a condition of employment or continued employment. An employer who violates this law shall be subject to criminal penalties and civil liability.