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Night Biomedical Product Development Engineer Jobs

Bachelor's degree in Biomedical, Mechanical or Chemical Engineering or equivalent * 3+ years of full-time experience in a product development role within the medical device industry * Experience ...

Bachelor's degree in chemical engineering, mechanical engineering, biomedical engineering, or ... product development environment * Ability to learn manufacturing process development ...

Bachelor's degree in chemical engineering, mechanical engineering, biomedical engineering, or ... product development environment * Ability to learn manufacturing process development ...

We are seeking a Product Development Engineer to work within MilliporeSigma Process Solutions ... Bachelor's degree in Mechanical Engineering, Chemical Engineering, Biomedical Engineering, Material ...

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Night Biomedical Product Development Engineer information

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$39.5K

$87.9K

$132.5K

How much do night biomedical product development engineer jobs pay per year?

As of Jun 9, 2026, the average yearly pay for night biomedical product development engineer in the United States is $87,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,000.00 and $100,000.00 per year, depending on experience, location, and employer.
What are the most commonly searched types of Biomedical Product Development Engineer jobs? The most popular types of Biomedical Product Development Engineer jobs are:
Product Development Engineer

Product Development Engineer

Intellectt INC

Minnetonka, MN • On-site

Contractor

Posted 18 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.