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Intern Biomedical Product Development Engineer Jobs in Minnesota

Henkel

Product Development Engineer

Cannon Falls, MN · On-site

$75K - $110K/yr

The Product Development Engineer is responsible for the scale-up of newly developed multi-million-dollar thermal interface material product lines used in a variety of industrial applications. * Works ...

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Intern Biomedical Product Development Engineer information

What is the difference between Intern Biomedical Product Development Engineer vs Intern Biomedical Research Associate?

AspectIntern Biomedical Product Development EngineerIntern Biomedical Research Associate
Required CredentialsEnrolled in or recent graduate of biomedical engineering, bioengineering, or related fieldsEnrolled in or recent graduate of biology, life sciences, or related fields
Work EnvironmentProduct development labs, engineering teams, cross-functional collaborationResearch labs, academic or clinical research settings
Employer & Industry UsageMedical device companies, biotech firms, healthcare product developmentResearch institutions, pharmaceutical companies, academic labs

The main difference is that the Intern Biomedical Product Development Engineer focuses on designing and developing medical devices and products, while the Intern Biomedical Research Associate is involved in conducting scientific research and experiments. Both roles require relevant educational backgrounds and are common in biomedical industries, but they serve different stages of product lifecycle and research focus.

What cities in Minnesota are hiring for Intern Biomedical Product Development Engineer jobs? Cities in Minnesota with the most Intern Biomedical Product Development Engineer job openings:
Intern Biomedical Product Development Engineer jobs near you
Product Development Engineer

Product Development Engineer

Intellectt INC

Minnetonka, MN • On-site

Contractor

Posted 5 days ago

Job description

Job title: Product Development Engineer
Location: Minnetonka, MN
Duration: 12 Months
 
Job Summary

The Product Development Engineer supports new product development and commercialization by executing engineering tasks, testing, documentation, data analysis, equipment qualification, and design control activities in a regulated medical/pharmaceutical environment.

Key Responsibilities

  • Support new product development using engineering fundamentals.
  • Install, qualify, and support R&D equipment.
  • Perform engineering testing, data analysis, and technical report writing.
  • Develop and validate test methods for materials and inspections.
  • Maintain Design History Files (DHF) and support DFMEA/risk management.
  • Prepare DMR documentation such as specifications, test methods, and manufacturing instructions.
  • Participate in design reviews, root cause analysis, and failure investigations.
  • Support technology transfer and process validation for new product launch.
  • Ensure compliance with FDA regulations, and safety procedures.

Required Skills

  • BS in Engineering; Mechanical or Biomedical preferred.
  • Good understanding of design control and quality systems.
  • Knowledge of statistics: Gage R&R, capability analysis, DoE, normality, acceptance sampling.
  • Experience with technical writing and data analysis.
  • Familiarity with FDA-regulated environments: 21 CFR 211, 21 CFR 820, ISO 13485.
  • Knowledge of root cause analysis tools like 5 Whys and Ishikawa.
  • Proficiency in Excel/Minitab.

For more information, please reach out at 732-719-4936 or share your updated resume with padma.priya@intellectt.com.