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Temporary Biomedical Product Development Engineer Jobs in Massachusetts

$35 - $41/hr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

Biomedical Engineer Location: Burlington, MA, 100% Onsite Duration: 6+ months Responsibilities ... Works cross functionally and collaboratively with Product Development, Engineering, Manufacturing ...

Reporting to the Director of Manufacturing, the Senior Product Development Engineer will lead efforts to create and commercialize groundbreaking products, and serve as a key contributor to the growth ...

Production Assembler II

Norwood, MA

$22 - $25/hr

  • Medical

  • Dental

  • Vision

  • Retirement

  • PTO

Nova Biomedical: One Global Brand. One Vision. Together under one name. Advanced Instruments and ... Collaborate with Engineering and provide feedback to support process and product development ...

Biomedical Market Manager

Norwood, MA · On-site

$130K - $150K/yr

The Market Manager will contribute to the early phases of new product development by leading ... or Engineering as well as approximately 1-3 years of marketing, product/market management and/or ...

Showing results 21-40

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 Massachusetts?

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

$35 - $41/hr

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Re-posted 12 days ago


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Company rating: 7.8 out of 10

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Job description

Apply Category: Engineering & Scientific, Engineering Title: Biomedical Engineer Location: Burlington, MA, 100% Onsite Duration: 6+ months Responsibilities: Perform failure analysis on explanted biomedical implant product. Provide technical expertise to the Product Analysis Laboratory. Analyzes failures, develops, and implements investigative protocols to identify root causes, performs circuit analysis, performs device and component level failure analysis.

Perform failure analysis on explanted long-term biomedical implant product. Work requires the application of theoretical principals, evaluation, ingenuity, and creative/analytical techniques to identify route cause failure mechanisms. Must be able to meet deadlines on multiple assignments and be able to operate in a diverse cross-functional team environment.

Proactive in finding quality improvements related to Failure Analysis May serve as lead and assign work to less experienced personnel and serves as a mentor when assisting less experienced lab staff in solving more complex problems. Works cross functionally and collaboratively with Product Development, Engineering, Manufacturing, and Product Surveillance. Aides in definition of test equipment as required to accomplish quality responsibilities.

Support all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements. Complies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments

Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors. Qualifications Bachelor's Degree in Engineering is Required Electrical or Biomedical Engineering is preferred Engineering work experience is preferred Knowledge of global regulations for medical device reporting and medical terminology is a positive Strong written and oral communication skills are required Candidate must be able to work well independently and on teams in a busy department while managing multiple ongoing tasks and investigations simultaneously Multitasks, prioritizes, and meets deadlines in a timely manner Strong organizational and follow-up skills, as well as attention to detail. Consultants Eligible Benefits Upon Waiting Period: Medical and Prescription Drug Plans Dental Plan Vision Plan Health Savings Account (for High-Deductible Health Plans) Flexible Spending Accounts (Health, Limited Purpose, Dependent Care, Commuter Parking and Commuter Transit) Supplemental Life Insurance Short Term Disability (coverage varies by state) Long Term Disability Critical Illness, Hospital coverage, Accident Insurance MetLife Legal, MetLife ID Fraud, and MetLife Pet Insurance 401(k) Abbott is a global healthcare leader that helps people live more fully at all stages of life.

Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritional and branded generic medicines. Working together, Abbott and Talent Solutions partner to deliver top talent for contingent roles at Abbott, building better and healthier lives. Abbott believes all employees are essential to creating life-changing breakthroughs, performing key duties to create life-changing breakthroughs.

Published on 06 Jul 2026, 8:52 PM


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