Associate Toxicologist

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 Med Tech solutions that advance global healthcare, improve patient lives and accelerate Client success and the Mission to deliver best-in-class global Med Tech development solutions through our people, expertise and technology by adhering to our core Values:
Act with integrity in everything we do. Provide best-in-class customer experiences. Develop superior talent and deliver expertise. Respond with agility and provide timely results. Embrace collaboration, diverse perspectives and ideas.

Compensation Target: $75,000.00

• Participate in meetings with prospective clients
• Provide scope of project and relevant information to support the creation of proposals
• Offer opportunities to clients for expansion of services to be provided by NAMSA
• Prepare risk assessments, evaluation plans and reports, in compliance with ISO 10993-1 ISO 10993-17 and ISO 14971, for submissions to FDA and other regulatory agencies
• Evaluate and summarize biocompatibility and general toxicology data ensuring compliance with the relevant regulatory requirements and standards
• Working knowledge of FDA medical device regulations and/or biologics regulations, ISO 10993 series, and 14971
• Ensure biocompatibility studies are in compliance with most recent regulatory requirements
• Provide technical support to lab staff
• Advise clients on technical issues related to biocompatibility and material characterization
• Perform biocompatibility gap analyses and write clear concise reports
• Performs and summarize literature searches
• Facilitate the collection of test data from other NAMSA entities as they relate to a specific project
• Establish and ensure schedule, budget and quality commitments are met for the client
• Evaluate and determine biological relevance of unexpected results
• Understand investigational product(s) and high level understanding of the Medical Device Development Process.
• Handle challenging situations, and know when to call-in help.
• Interact as needed with clients, auditors, inspectors, subcontractors, consultants, and other individuals or departments
• Author blog posts or white papers
• Summarize testing reports for submissions
• Able to identify and evaluate Standards and Guidance Documents applicable to client’s device
• Other duties as assigned

• Bachelor’s degree or equivalent experience in a related field, and a minimum of 5 years of relevant experience; or Masters or Doctorate degree, and a minimum of 2 years of relevant experience required
• Fluency in English and local language, if different, required
• Knowledge and experience with applicable standards and regulations for medical devices
• Ability to assess/audit compliance of biocompatibility and material characterization results to applicable standards and regulations
• Ability to develop biological safety documents and reports that are compliant with applicable standards and regulations
• Knowledge of and experience with Microsoft Word
• Write and review complex documents

• The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable…