
NAMSA pioneered the industry and was the first independent company in the world to focus solely on medical device materials for safety. NAMSA started testing medical devices before the U.S. Food and Drug Administration started regulating such products in 1976.
We are shaping the industry. NAMSA has been a key contributor to the development of the test methods that govern our industry. We have become the industry’s premier provider. We provide support for clients during every step of the product development lifecycle and beyond.
Come and work for an organization with the:
Vision to inspire innovative MedTech solutions that advance global healthcare, improve patient lives and accelerate Client success and the
Mission to deliver best-in-class global MedTech development solutions through our people, expertise and technology by adhering to our core
$185,000.00
NAMSA | Future Career Opportunities
Location: Onsite (MN and OH) and Remote Opportunities, Depending on Role
Career Levels: Entry-Level through Principal Technical Expert
Compensation: Varied by Role
Build Your Career in Pathology at NAMSA
At NAMSA, our Pathology professionals play a critical role in advancing medical device safety and innovation. As a global leader in medical device testing and development, we offer opportunities for scientific professionals to contribute to meaningful research that improves patient lives.
We invite individuals at all career stages, from entry-level laboratory support through advanced scientific expertise, to join our Pathology Talent Building Community and explore future career opportunities.
Explore Our Pathology Career Opportunities
Our Pathology career opportunities include the following positions, listed from entry-level through our most advanced technical roles.
Supports pathology laboratory operations, including necropsy preparation, specimen handling, tissue archiving, imaging, and laboratory maintenance.
Basic Qualifications:
High school diploma required. Associate's or bachelor's degree, or related coursework in biological or animal sciences, preferred.
Animal laboratory experience preferred.
Supports necropsy procedures, gross examinations, tissue trimming, specimen processing, and laboratory documentation in a GLP-regulated environment.
Basic Qualifications:
Associate's or bachelor's degree in Biological Sciences or a related discipline; OR Two years of laboratory experience with AALAS ALAT certification or certification eligibility within six months.
GLP nonclinical pathology experience preferred.
Independently performs necropsies, gross examinations, tissue trimming, and specimen management while supporting study activities and GLP compliance.
Basic Qualifications:
Associate's or bachelor's degree, or equivalent, in Biological Sciences or a related discipline. Minimum three years of experience in a GLP nonclinical environment.
Supports pathology study deliverables, protocol reviews, scientific reporting, digital slide imaging, and computer-assisted morphometry.
Basic Qualifications:
Associate's or bachelor's degree in Biological Sciences or a related discipline.
Minimum two years of experience in a GLP preclinical pathology environment.
Strong computer and communication skills with knowledge of FDA, GLP, and ISO regulations.
Independently performs advanced necropsy and gross pathology procedures, coordinates laboratory workflows, trains technicians, and supports operational improvements.
Basic Qualifications:
Associate's or bachelor's degree, or equivalent, in Biological Sciences or a related discipline. Minimum five years of experience in a GLP nonclinical environment.
Serves as a study pathologist, interpreting gross and microscopic pathology findings, developing pathology methodologies, and preparing scientific reports supporting nonclinical research.
Basic Qualifications:
Doctor of Veterinary Medicine (DVM) or Medical Doctor (MD).
Minimum three years of related experience emphasizing toxicologic or implant pathology. ACVP, ECVP, or equivalent board certification desired.
Provides advanced pathology interpretation, scientific consultation, technical guidance, and specialized expertise supporting complex nonclinical studies and regulatory submissions.
Basic Qualifications:
DVM or MD degree. Minimum six years of relevant experience in implantable medical device pathology, toxicologic pathology, or related industry applications. ACVP, ECVP, or equivalent board certification desired. Demonstrated scientific writing, analytical, and project management skills.
Serves as a senior scientific expert, providing specialized pathology consultation, technical leadership, advanced study interpretation, and scientific innovation supporting medical device research.
Basic Qualifications:
DVM or MD degree. ACVP, ECVP, or equivalent board certification required. Minimum eight years of relevant implantable medical device pathology, toxicologic pathology, or related industry experience. Demonstrated scientific expertise, statistical and analytical capabilities, and regulatory or publication experience.
Why Join NAMSA?
Contribute to innovative medical device research and patient safety.
Collaborate with experienced scientific and technical professionals.
Explore career advancement from laboratory operations to advanced pathology expertise. Make a meaningful impact on medical technology development.
Interested in Opportunities Available Now?
We encourage you to explore our current job openings and apply directly to any active requisitions that align with your qualifications and career interests.
CLICK HERE TO VIEW ALL ACTIVE NAMSA CAREER OPPORTUNITIES
All qualifications are listed above.
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The compensation grade range for this position is:
$124,800.00 - $242,800.00
Annual
Please Note: Individual base pay depends on various factors, in addition to primary work location, such as complexity and responsibility of role, job duties/requirements, and relevant experience and skills.

Helping medical device Sponsors improve healthcare since 1967, NAMSA is the world’s leading MedTech Contract Research Organization (CRO) offering global end-to-end development services. Driven by its global regulatory expertise and in-depth therapeutic knowledge, NAMSA is dedicated to accelerating medical device product development, offering only the most proven solutions to move clients’ products through the development lifecycle efficiently and cost-effectively. From medical device testing; regulatory, reimbursement and quality consulting; and clinical research services, NAMSA is the industry’s premier, trusted partner for successful development and commercialization outcomes. Learn more: https://namsa.com/about/client-testimonials/