R&D Engineer II

Posted 7 Days Ago
Be an Early Applicant
Maple Grove, MN
In-Office
75K-100K Annually
Mid level
Healthtech
The Role
The R&D Engineer II at NPX Medical manages customer projects, designs products, and ensures compliance with quality standards. Responsibilities include project management, equipment procurement, and developing inspection procedures.
Summary Generated by Built In

An engineer at NPX Medical is responsible for solving technical issues for customers. This may be anything from new product

designs to manufacturing/quality issues. He/she helps establish specifications to ensure products conform to performance

and quality standards. He/she works directly with QA to define and implement inspection activities and to enforce

requirements as specified by design specifications and regulatory agencies. An engineer is responsible for following the

established GMP/ISO/MDD compliant quality system practices as requested by the customer.

RESPONSIBILITIES:

  • Manage customer projects and communication between NPX Medical and customers.
  • Manage project goals and expectations with customers.
  • Design and develop products and processes in various fields for NPX Medical customers.
  • Provide project plans and reports as to project status.
  • Evaluate and procure equipment necessary to manufacture products. Contact and communicate with outside vendors for parts and/or services that are required by NPX Medical customers but cannot be performed by NPX Medical.
  • Specify materials and processes to ensure the continued performance and compliance of products.
  • Coordinate and supervise product/project scale-up during all transitions from design to production.
  • Define and develop inspection procedures and tests to ensure product specifications are met.
  • Define and develop qualification plans for products based on performance specifications and design prints.
  • Provide technical assistance for diagnosing manufacturing and quality problems.
  • Conduct technical and statistical investigations concerning quality problems.
  • Develops and documents test plan protocols, standard operating procedures, specifications and test procedures.
  • Perform systems validation.
  • Review quality system changes pertaining to Engineering and Supply Chain.
  • Provide training to operators for engineering documentation, including but not limited to: procedures, forms and traceability control forms.

Requirements
  • Four-year degree in a technical discipline, ideally in mechanical, manufacturing, or industrial quality engineering.
  • At least three (3) years of post-graduate experience in a technical or engineering role.
  • Strong oral and written communication skills.

Benefits
  • Compensation: The expected salary for this position is between $75,000-$100,000 annually, depending on experience, skills, qualifications.
  • Health Care Plan (Medical, Dental & Vision)
  • Retirement Plan with Company Match
  • Paid Time Off, Personal Days, AND Birthday Holiday!
  • Lifetime Membership Subsidy and Wellness Resources
  • Life Insurance (Basic, Voluntary & AD&D)
  • Family Leave (Maternity, Paternity)
  • Short-Term & Long-Term Disability
  • Taco Thursdays!!!

Top Skills

Gmp
Iso
Mdd
Quality Engineering
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The Company
HQ: White Bear Lake, MN
172 Employees
Year Founded: 2000

What We Do

Nextern collaborates with innovators, clinicians, and device partners to create, iterate, optimize and manufacture best-in-class medical devices. We bring an unmatched core competence in medical device product design and development through manufacturing as a leverageable asset to collaborators like you, who are focused on accelerating the commercial side of the business.​

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