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New

Sr. Process Molding Engineer

Cirtec Medical
paid time off, 401(k)
United States, Minnesota, Brooklyn Park
9315 Winnetka Avenue North (Show on map)
May 15, 2026

Description

About us:

For over three decades, Cirtec Medical has been a leading outsourcing partner for complex medical devices. We specialize in providing comprehensive solutions for Class II and III devices, from design and development to precision components and finished device assembly. Our expertise spans neuromodulation, implantable drug delivery, cardiac rhythm management, structural heart, mechanical circulatory support, and minimally invasive surgical systems.

Our dedicated teams prioritize growth, innovation, and collaboration. We actively seek opportunities for improvement to enhance our support for clients. If you embrace a growth mindset and thrive on challenges, you may be a perfect fit for our team!

Position Summary:

The Sr. Process Molding Engineer position is primarily responsible for the design, development, implementation, and optimization of injection molding processes and equipment for new and existing medical device production lines. This role applies advanced silicone, plastics, and scientific molding principles to improve safety, quality, delivery, and cost while ensuring compliance with applicable medical device quality and regulatory requirements. The position works crossfunctionally within a project engineering environment and supports, process development, qualification, validation, and manufacturing transfer activities.

Key Responsibilities:

  • Design, detail, and implement injection molding process and equipment solutions that improve safety, quality, delivery, and cost for new and existing molding production lines.
  • Utilize indepth knowledge of injection molding, resins, silicones, and plastics processing to develop molds, tooling, fixtures, and auxiliary equipment that optimize productivity, maintainability, and total cost of ownership.
  • Apply scientific molding principles to define, characterize, and optimize molding processes, including mold tool qualifications, process characterization window studies, and molding process qualifications.
  • Define, prepare, and implement engineering and production documentation, including equipment qualifications (IQ/OQ/PQ), process and work instructions, and technical reports.
  • Troubleshoot injection molding machines, molding processes, tooling issues, and molded part defects using scientific molding tools and datadriven problemsolving methods; develop corrective action plans with defined timelines and followthrough.
  • Support process failure mode and effects analysis (pFMEA), risk assessments, and continuous improvement initiatives related to molding operations.
  • Collaborate with Development Engineers, Tool Makers, Team Leaders, Technicians, Customers, and Suppliers to evaluate and influence product and process designs for manufacturability, quality, and cost reduction.
  • Support feasibility builds, prototype tooling, equipment selection, and process development activities for new products.
  • Provide technical support during design verification, clinical builds, training builds, process validation, and manufacturing transfer to production.
  • Provide technical guidance and mentoring to technicians and associates on injection molding processes, equipment operation, and process control.
  • Track and communicate project status related to molding activities, including risks, issues, timelines, and deliverables.

Must Have:

  • Bachelor's degree in Engineering required (Mechanical, Manufacturing, or related STEM discipline preferred) and 5+ years of relevant molding experience.
  • Demonstrated experience with injection molding processes, tooling, and materials, preferably in a regulated medical device manufacturing environment (Class II and/or Class III)
  • Working knowledge of scientific molding methodologies, including DOE, process characterization, and robust process development.
  • Experience with mold qualifications, process validations, and medical device quality system requirements.
  • Ability to read, interpret, and create technical drawings, blueprints, specifications, and process documentation.
  • Strong analytical, troubleshooting, and problemsolving skills.
  • Demonstrated ability to work effectively in crossfunctional teams and communicate technical information clearly.
  • Proficiency with standard computer tools, including MS Office applications; familiarity with CAD and statistical tools preferred.
  • Must maintain high ethical standards and demonstrate good organizational and timemanagement skills.
  • Ability to train and support technicians and other engineering personnel on moldingrelated activities.
  • Must be able to read, write, and speak fluent English.
  • Willingness to travel, if required.

Salary Range: 100,000 to 132,000 based on skills and experience

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.

We work to create a culture that is built on innovation, respect, transparency and communication, and hope you take pride in being a member of our team. It is Cirtec's goal to create a great work environment and to keep the company a great place to work. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Our benefits include Training and career development, Healthcare and well-being programs including medical, dental, vision, wellness and occupational health programs, Paid Time Off and 401(k) retirement savings with a company match.

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