Principal Process Development Engineer - IPG at RESOLUTION MEDICAL LLC

Minneapolis, Minnesota, United States -

Full Time

Start Date

Immediate

Expiry Date

14 Jul, 26

Salary

185000.0

Posted On

15 Apr, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Process development, Medical device manufacturing, Active implantable devices, Neuromodulation, Process validation, Laser welding, Helium leak testing, Design for manufacturing, Design control, Quality systems, SolidWorks, Mastercam, Lean manufacturing, Project management, Equipment validation, Capital expenditure justification

Industry

Medical Device

Description

Description Job Summary The Principal NPI/Process Development Engineer position leads the development, improvements and implementation of optimal cost-effective designs and associated processes that meet the high rigor of product requirements and exceptional quality standards. This role will work specifically with active implantable products. Essential Functions Works independently to drive project completion by developing the processes used to manufacture component, sub-assemblies, and FG devices. Provides leadership and mentors less experienced engineers and technicians. Acts as the liaison between development and operations. Advocates for the process to ensure they are repeatable and can capably produce product that meets the design requirements. Prepares and presents detailed plans necessary to complete assigned projects. Develops schedule milestones, coordinates resources, facility and equipment for assigned projects. Assists in improving the system of production controls, standard operating procedures, safety, quality control and training. Prepares and maintains detailed layouts of buildings and equipment. Coordinates the manufacturing launch of new/revised products including establishing goals, training team members and evaluating results. Designs, develops and tests as well as sources various tools, machinery and equipment for recommended manufacturing methods while providing ROI analysis. Performs product/process analysis for production and quality metrics. Write engineering change orders to process changes to manufacturing documents, drawing, and Bill of Materials. Support company finance, accounting, human resources, quality, regulatory, and clinical departments as necessary to ensure compliance with requirements. Recommend, support and implement improvements, modifications, or additions that will improve work processes. Take the lead in analyzing the need for new process development and to meet company needs including specifying, ordering, installing and validating new equipment or processes. Prepares justification for capital expenditures. Aid in production transfers from R&D to manufacturing. Propose potential new manufacturing technologies, including automation and new equipment. Contribute to the definition, development and implementation of LEAN manufacturing initiatives. Requirements Education, Experience, Required Skills Bachelor’s degree in engineering or related field 10+ years related experience in medical device industry with a heavy focus on product or process development of Active Implantable Devices. Strongly preferred experience in Neuromodulation Devices (IPGs or Leads). Experience with pacemakers, cardiac monitors, brain computer interface, etc. also considered. Extensive experience with process validations for laser welding, header attachment, and internal moisture (bake) and Test Method Validation for Helium Leak Testing. Demonstrated ability to independently develop medical device manufacturing processes from concept to production. Experience with medical device Design For Manufacturing, design control, quality systems and product development phases. Demonstrated ability to implement change in a way that positively impacts overall department and company performance. Must be able to handle multiple projects simultaneously. Must excel at working in a team environment with a high level of people/interpersonal skills and demonstrated ability to cross functionally drive results. Experience using influence to affect project and organizational success. Experience with programs including SolidWorks and/or Mastercam. MS Office Proficiency. Ability to handle and be trusted with confidential and/or sensitive information. Physical Requirements Prolonged periods of sitting at a desk and working on a computer. Must be able to lift up to 25 pounds at times. Must have excellent hand-eye coordination. Ability to differentiate between colored wires, tabs, and electronic components. Must wear gown, gloves, and ear protection if applicable. Summary of Benefits Group health & welfare benefits: Options for Medical, Dental and Vision insurance, Health Savings Account (requires participation in eligible medical plan), and Flexible Spending Accounts. Company-paid benefits: Employee Life Insurance & Accidental Death & Dismemberment (AD&D), Long Term Disability (LTD), Kavira (requires participation in medical plan). Voluntary, employee-paid benefits: Employee Supplemental Life & AD&D, Spouse and Dependent Life & AD&D, Short Term Disability (STD), Accident, Critical Illness, and Hospital Indemnity, Employee Assistance Program. Flexible Time Off Program Paid Parental Leave Paid Holidays Benefits and incentive compensation may be subject to generally applicable eligibility, waiting period, contribution, and other requirements and conditions. Compensation The typical base pay range for this role is between $135,000-185,000/year. Compensation may vary based on individual job-related knowledge, skills, expertise, and experience. This position is eligible for a discretionary annual incentive program driven by organization and individual performance.

Responsibilities

The Principal Process Development Engineer leads the development and implementation of cost-effective manufacturing processes for active implantable medical devices. This role acts as a liaison between R&D and operations to ensure production quality, repeatability, and compliance with regulatory standards.