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Mechanical R&D Engineer; Entry​/Junior Level - Medical Devices

Job in Minneapolis, Hennepin County, Minnesota, 55400, USA
Listing for: Planet Pharma
Full Time position
Listed on 2026-03-08
Job specializations:
  • Engineering
    Quality Engineering, Mechanical Engineer, Manufacturing Engineer, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 80000 - 100000 USD Yearly USD 80000.00 100000.00 YEAR
Job Description & How to Apply Below
Position: Mechanical R&D Engineer (Entry/Junior Level) - Medical Devices

Our client, a leading Medical Device company, is seeking an entry/junior level Mechanical R&D Engineer to join its growing team. Please note that this role is 100% onsite in the Maple Plain area. Please only apply if you are able to commute there daily. See below for other info!

Top Skills Needed:

  • Equipment:
    Laser scanning;
    Micro View

Responsibilities:

  • The R&D Component Engineer I will be a key member of the engineering team, partnering with representatives from R&D, Quality, Supply Chain, and Production.
  • This position is responsible for evaluating and dispositioning mechanical components used in the manufacturing scale up of medical device products.
  • The R&D Component Engineer I acts as the technical bridge between design, procurement, and manufacturing, ensuring every mechanical part that goes into the instruments will be functional, reliable, compliant, and cost-effective.
  • In all actions, the R&D Component Engineer I shall demonstrate a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented processes and procedures.
  • Evaluating and approving parts to ensure compliance with requirements
  • Inspect, analyze, potentially rework, review, test and disposition components to ensure functionality
  • Perform both design and project tasks related to the inspection, testing, and production support of implantable orthopedic devices and associated non-implantable delivery instruments
  • Assist in research and development of new components, assemblies, and processes to support product development and continuation activities
  • Perform dimensional, strength of materials, mechanism movement, and/or manufacturability analysis
  • Generate test methods and protocols, perform tests, analyze data, generate reports for product verification, and present findings as needed to cross-functional stakeholders
  • Create and support documentation activities including, but not limited to: drawings and specifications for piece parts and assemblies; generate change orders to existing documents; review documentation generated by others related to product responsibilities; actively participate in design reviews; document the appropriate development and manufacturing practices per quality system or internal requirements; and verify all final design documentation, parts lists, and drawings to ensure compliance and accuracy
  • Perform various product engineering tasks as necessary to support R&D and operations
  • Communicate updates to the program manager and other various cross-functional team members as it relates to task completion and schedule adherence relative to overall business goals and objectives
  • Evaluate and solve technical challenges either individually or as part of a team by: collaborating cross-functionally to troubleshoot issues and implement solutions; actively participating in problem solving sessions and/or brainstorming; systemically and logically working through issues using personal skills/experience and/or pulling in resources as needed; and designing and conducting experimental testing to appropriately characterize and evaluate solutions
  • Participate in engineering meetings, technical working groups, and project management discussions
  • Assist in the building, prototyping, modifying, and testing of engineering components
  • Assist with prototyping, assembling, characterizing, validating inspection processes, rework instructions, and/or test methods
  • Follow safety protocols, quality SOP’s, and regulatory requirements in all tasks and activities
  • Comply with applicable design-related standards published by external regulatory bodies
  • Properly document activities in accordance with best engineering practices, company procedures, and regulatory requirements
  • Perform other duties as needed and assigned

Requirements:

  • Bachelor’s degree in engineering (Mechanical, Manufacturing, Industrial, Biomedical, or technical equivalent) with 0-3 years of related work experience or an equivalent combination
  • Hands-on experience in metrology and familiarity with metrological equipment
  • Experience in the use of analytical methods including statistics, DOE, and associated SW tools (Minitab)
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