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Temporary Biomedical Product Development Engineer Jobs

Coloplast

Product Development Engineer

Minneapolis, MN

$90K - $120K/yr

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 ...

Solesis

Product Development Engineer

Apex, NC

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

First Quality

Product Development Engineer

Macon, GA · On-site

We are seeking a Product Development Engineer for our First Quality Baby Products facility located ... Chemical, Biomedical, or Mechanical Engineering) or equivalent; additional business studies ...

Merck Group

Product Development Engineer III

Bedford, MA

$84K - $127K/yr

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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Temporary Biomedical Product Development Engineer information

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$39.5K

$87.9K

$132.5K

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

As of Jun 23, 2026, the average yearly pay for temporary 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.

Is BME a stressful job?

A Temporary Biomedical Product Development Engineer role can be stressful due to tight project deadlines, the need for precision, and regulatory compliance requirements. The job often involves problem-solving, collaboration, and working with complex medical devices, which can contribute to workload pressure. However, stress levels vary depending on workload management and workplace environment.

What are Temporary Biomedical Product Development Engineers?

Temporary Biomedical Product Development Engineers are professionals who work on a contract or short-term basis to design, develop, and improve medical devices or products. They collaborate with cross-functional teams to ensure products meet regulatory standards, are safe for patients, and perform as intended. Their duties may include prototyping, testing, documentation, and supporting the transition from concept to manufacturing. These roles are often found in medical device companies during periods of increased workload or for specific projects. Temporary positions allow companies to bring in specialized expertise for a limited time.

What are the key skills and qualifications needed to thrive as a Temporary Biomedical Product Development Engineer, and why are they important?

To excel as a Temporary Biomedical Product Development Engineer, you need a strong background in biomedical engineering principles, product design, and regulatory standards, typically supported by a relevant engineering degree. Familiarity with CAD software (like SolidWorks), rapid prototyping tools, and knowledge of FDA or ISO regulations are commonly required. Strong analytical thinking, collaboration, and adaptability are crucial soft skills for success in cross-functional teams and fast-paced projects. These skills and qualifications are important to ensure safe, effective, and compliant product development within tight project timelines.

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

AspectTemporary Biomedical Product Development EngineerTemporary Biomedical Research Associate
CredentialsBachelor's or Master's in Biomedical Engineering or related fieldBachelor's or Master's in Biology, Biomedical Science, or related field
Work EnvironmentProduct design labs, R&D departments, manufacturing settingsResearch labs, clinical trial sites, academic institutions
Employer & Industry UsageMedical device companies, biotech firms, pharmaceutical companiesResearch institutions, hospitals, biotech research labs

The Temporary Biomedical Product Development Engineer focuses on designing and developing medical devices and products, often working in R&D and manufacturing environments. In contrast, the Temporary Biomedical Research Associate primarily conducts experiments and supports research projects in labs. Both roles require relevant scientific credentials but differ in their focus on product development versus research activities.

What engineers make $500,000?

Highly experienced biomedical product development engineers working in senior roles, management, or specialized consulting can earn salaries approaching or exceeding $500,000 annually, especially with bonuses and stock options. Such compensation typically requires advanced skills, extensive industry experience, and often leadership responsibilities in the medical device or biotech sectors.

What engineers make $300,000 a year?

Senior biomedical product development engineers with extensive experience, specialized skills, and advanced certifications can earn salaries approaching or exceeding $300,000 annually, especially in leadership roles or high-demand sectors. Compensation often depends on factors such as location, company size, and industry demand for expertise in areas like device design, regulatory compliance, and project management.

Can biomedical engineers make 200k?

Biomedical engineers, including those in product development roles, typically earn salaries below $200,000 annually, with higher earnings often associated with senior positions, specialized skills, or management responsibilities. Achieving a $200,000 salary may require extensive experience, advanced degrees, or working in high-paying industries or locations.

What types of projects and collaboration can a Temporary Biomedical Product Development Engineer expect during their assignment?

As a Temporary Biomedical Product Development Engineer, you will likely be involved in specific phases of the product lifecycle such as prototyping, testing, or design improvements, depending on the organization's current needs. You will work closely with cross-functional teams—including R&D scientists, quality assurance, manufacturing, and regulatory affairs—to ensure that products meet both technical and compliance standards. Temporary roles often require adaptability, as project priorities can shift quickly, and you may be asked to contribute to multiple initiatives. This collaborative environment offers exposure to various aspects of biomedical engineering and can help expand your professional network.
What cities are hiring for Temporary Biomedical Product Development Engineer jobs? Cities with the most Temporary Biomedical Product Development Engineer job openings:
What are the most commonly searched types of Biomedical Product Development Engineer jobs? The most popular types of Biomedical Product Development Engineer jobs are:
What states have the most Temporary Biomedical Product Development Engineer jobs? States with the most job openings for Temporary Biomedical Product Development Engineer jobs include:
Temporary Biomedical Product Development Engineer jobs near you
Product Development Engineer

Product Development Engineer

Intellectt INC

Minnetonka, MN • On-site

Contractor

Posted 2 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.