Biomedical Associate (Ph.D.)

ExponentPhiladelphia, PA
Onsite

About The Position

Exponent is seeking a Biomedical Associate for its Biomedical Engineering and Sciences Practice in Philadelphia, PA. This role involves working within a team to address complex challenges for clients in the medical device and life sciences sectors, focusing on both regulatory consulting and litigation support. The position requires an advanced degree (Ph.D.) with a background in mechanical engineering and cell and molecular biology, along with practical experience in developing laboratory test systems for evaluating medical devices or physiological systems.

Requirements

  • Ph.D. (or equivalent) in Mechanical Engineering, Biomedical Engineering, or a closely related field.
  • Academic training in cell and molecular biology, with practical laboratory experience in cell-based or biological assays.
  • Demonstrated experience developing and validating test systems or experimental rigs for evaluating product or physiological performance in a laboratory setting.
  • Working knowledge of cardiopulmonary physiology and the mechanical and biological behavior of cardiovascular and respiratory systems.
  • Excellent written and verbal communication skills.
  • Superior problem-solving abilities and strong attention to detail.
  • Strong educational and publication credentials.
  • Strong teamwork and leadership skills.

Nice To Haves

  • Familiarity with FDA regulatory frameworks for medical devices (e.g., 21 CFR, design controls, biocompatibility standards) is a plus.
  • Experience applicable to medical device development, regulatory testing, or failure analysis is highly desirable.

Responsibilities

  • Designing, developing, and executing laboratory test systems and experimental protocols to evaluate the performance and safety of medical devices, with particular emphasis on cardiovascular and pulmonary applications.
  • Performing technical evaluations, scientific analysis, and testing on behalf of medical device companies in support of FDA regulatory submissions and compliance activities.
  • Supporting product liability litigation and intellectual property matters through technical analysis, root cause investigation, and expert report preparation.
  • Gathering and synthesizing scientific and engineering information to convey technical conclusions to audiences in engineering, business, law, and industry.
  • Writing technical reports for regulatory agencies, industry clients, and litigation matters.
  • Publishing at conferences and in peer-reviewed literature.
  • Assisting in marketing the group's technical capabilities to clients and the scientific community.
  • Developing additional expertise and industry exposure through Exponent's unique technical consulting model.

Benefits

  • Competitive benefits
  • Compensation and recognition programs
  • Support for health and well-being

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Education Level

Ph.D. or professional degree

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