Associate Director
NAMSA
Associate Director
NAMSA
MedTech CRO delivering end-to-end device development
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
Values:
Compensation Target:
Job Description:
Job Profile SummaryQualifications & Technical Competencies:
Principal Duties and Responsibilities
Qualifications and Skills
Technical Competencies
Working Conditions
Working Conditions:
Position descriptions are not intended, and should not be construed to be an exhaustive list of all responsibilities, skills, and efforts or working conditions associated with a job. NAMSA reserves the right to revise duties as needed.
The compensation grade range for this position is:
$152,300.00 - $296,600.00-
AnnualPlease 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.
NAMSA is a medical device-focused contract research organization (CRO) that provides end-to-end development services. It helps sponsors bring medical devices to market by offering testing, regulatory and quality consulting, reimbursement support, and clinical research. The way it works is through a global team with regulatory expertise and therapeutic knowledge who guide and perform the work needed across the product development lifecycle, from initial testing to regulatory clearance, reimbursement, and commercialization. NAMSA differentiates itself with its worldwide regulatory know-how, depth of therapy-specific expertise, and a commitment to delivering proven, cost-effective solutions that speed up development. The company’s goal is to accelerate medical device product development and successful commercialization by providing comprehensive, reliable services and guidance from concept to market.
Explore more opportunities at NAMSA