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Temporary Biomedical Product Development Engineer Jobs in Missouri

Nestle

Product Development Associate

Saint Louis, MO

$65K - $84K/yr

Come prepared to handle various intermediate-term product developments and engineering processes for the business, as well as provide technical support to manufacturing operations. You'll leverage ...

Nood

Technical Product Development Manager

California, MO · On-site

$85 - $110/hr

Manage device development critical paths from industrial design through tooling, engineering validation, testing, certification, and first production run. * Oversee international manufacturing ...

EMSAR

Biomedical Equipment Engineer I

Kansas City, MO · On-site

Technical training and education Position Overview EMSAR is seeking a Biomedical Equipment Engineer ... Ability to develop productive working relationships with customers and colleagues at all levels.

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Temporary Biomedical Product Development Engineer information

What is a temporary biomedical product development engineer?

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?

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 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 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 are the most commonly searched types of Biomedical Product Development Engineer jobs in Missouri?

The most popular types of Biomedical Product Development Engineer jobs in Missouri are:

Temporary Biomedical Product Development Engineer jobs near you

New Product Development Design Engineer

Orscheln Industries

Moberly, MO • On-site

$114K - $137K/yr

Full-time

Re-posted 5 days ago

Job description

Work Eligibility:  Must be a U.S. Citizen or a permanent lawful resident of the U.S.

Summary:

Perform a variety of engineering tasks in design, development, verification, and troubleshooting of Orscheln electronic control and monitoring circuitry for powered equipment applications. The successful candidate will possess good communication skills, both verbal and written, the ability to interface with diverse individuals and groups, and strong planning and organizational abilities.

Preferred Educational Experience:

Bachelor’s degree in Electrical Engineering

Preferred Work Experience:

Applicable work experience will also be considered.  Preference will be given to candidates possessing a minimum of (3) years of related engineering in the area of electronic hardware design. Experience in electronics simulation, functional safety, automobile or commercial vehicle industry would be beneficial.

Essential Functions:

•         Work with customers both internal and external to develop design requirements.

•         Design, analyze, debug, verify, validate, and document hardware electronic assemblies following industry-standard design practices including functional safety (ISO26262).

•         Support existing products by analyzing circuits for potential applications/solutions.

•         Perform system and sub-system level safety analyses including Hazard Analyses, Fault Trees, and Failure Mode Effects and Criticality Analyses.

•         Perform schematic entry and either layout the board or work closely with a printed circuit board layout designer.

•         Perform and/or oversee the build-up, bring-up, debug, and low-level testing of electronic circuit board assemblies.

•         Define, execute, and document product verification and validation procedures (ISO26262).

•         Perform and/or work closely with software engineers and engineering technicians to test, debug, and verify the design.

•         Ability to perform all safety critical functions.

•         Must be able to understand and apply significant and critical characteristics on blueprints.

•         Follow all 6S & Safety Guidelines

o   Safety

o   Sort

o   Straighten

o   Scrub

o   Standardize

o   Sustain

Non-Essential Functions:

•         Perform all other tasks as assigned.

Qualifications and Desired Skills

  • Accomplished in the operation of:
    • DMM (Voltmeter/Ammeter)
    • Oscilloscope
    • Power Supply
    • Function Generator
    • CAN network communication and analysis devices
    • Automation equipment wiring/troubleshooting
  • Understanding of automotive specifications and requirements: ISO 26262, ISO 16750, CISPR 25, ISO 11452, SAE J1939
  • Office equipment
  • Computer skills
    • PADS/Mentor Graphics: Logic, Layout, Router.
    • Microsoft Office (Word, Excel, PowerPoint,  ..etc.)
  • Time management
  • Communication skills

Physical Requirements:

  • Data entry
  • 80% of the time sitting
  • Some bending/stooping
  • Lifting less than 35lbs
  • Climate controlled environment

AAP/EEO Statement:

It is the policy of Orscheln Products to provide equal employment opportunities without regard to race, color, religion, sex, national origin, age, disability, marital status, veteran status, sexual orientation, genetic information or any other protected characteristic under applicable law.

Employment Type: FULL_TIME

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