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Temporary Biomedical Product Development Engineer Jobs

Bachelor of Science or higher in Design, Industrial Design, Mechanical Engineering, Biomedical Engineering, or related field * Product development experience preferred Other Skills * Language skills:

Our customer in Adams County, IN is looking for a hands-on Product Development Engineer to support the design and improvement of industrial mechanical products used in manufacturing and automation ...

Our customer in Adams County, IN is looking for a hands-on Product Development Engineer to support the design and improvement of industrial mechanical products used in manufacturing and automation ...

As a Product Development Engineer, you will drive projects from concept through production launch, working closely with customers, manufacturing teams, and engineering stakeholders to develop high ...

Product Development Engineer - Asia Manufacturing (Mandarin-Speaking) Location: Onsite or Hybrid (Travel Required) Job Summary We are looking for a hands-on Product Development Engineer with a strong ...

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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 24, 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:
Senior Product Development Engineer

Senior Product Development Engineer

Femasys, Inc.

Suwanee, GA • On-site

Full-time

Posted 13 hours ago


Job description

We are looking for a Senior Product Development Engineer who thrives in a small, fast-paced environment and wants to play a hands-on role in bringing innovative medical devices from concept to market. This is not a narrowly defined role-you will be expected to take ownership, operate across design, testing, and development activities, and directly influence product and process outcomes.
Key Responsibilities:
  • Lead product development efforts from early concept through commercialization with a strong focus on execution.
  • Design and iterate components and assemblies using SolidWorks with minimal oversight.
  • Develop, build, and troubleshoot prototypes and test setups in a hands-on manner.
  • Design and qualify equipment (IQ/OQ/PQ) to support both development and early manufacturing.
  • Work closely with Manufacturing, Quality, and Regulatory to ensure practical, compliant solutions.
  • Identify issues quickly and drive resolution without relying on large support teams.
  • Generate and maintain design control documentation in alignment with FDA and ISO requirements.
  • Support design transfer and early production, including time on the manufacturing floor.

What We're Looking For:
  • An engineer who is comfortable operating with limited structure and high ownership.
  • A practical problem-solver who can balance speed with quality and compliance.
  • A team player who communicates directly and effectively in a small group setting.

Qualifications:
  • Bachelor's or Master's degree in Mechanical Engineering, Biomedical Engineering, or similar.
  • 5+ years of product development experience, ideally in the medical device industry.
  • Strong proficiency in SolidWorks.
  • Experience with equipment design and qualification (IQ/OQ/PQ).
  • Working knowledge of design controls and FDA/ISO 13485 requirements.
  • Demonstrated success in a small company, startup, or similar resource-constrained environment.

Preferred Experience:
  • Experience with catheter-based or minimally invasive devices.
  • Familiarity with processes such as extrusion, bonding, and assembly of disposable medical devices.
  • Experience supporting early manufacturing scale-up.