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NAMSA

MedTech CRO delivering end-to-end device development

Microbiology Technologist

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNorthwood, OH, USANo salary listedIn-person

About the Job

Requirements

  • A high school diploma or equivalent and at least two years of experience, or a bachelor's degree and no experience.
  • Sound judgment, effective decision-making skills, and the ability to solve problems or escalate as needed.
  • Awareness of applicable guidelines and regulations, including USP, ISO, CTFA, and FSA.
  • Knowledge of the metric system, NAMSA GLP and/or GMP testing, scientific applications, experimental design, and data evaluation.
  • Ability to work in a GLP/GMP environment.
  • Ability to maintain the physical condition necessary for prolonged walking, standing, or sitting.
  • Ability to use a computer keyboard extensively and operate computer equipment.

Responsibilities

  • Perform routine test article or product preparation, routine testing, and routine calculations in accordance with NAMSA standard operating procedures and work instructions, as applicable.
  • Collect and record raw data accurately in logbooks and on worksheets.
  • Check laboratory equipment and, when applicable, be on call and respond to continuous monitoring alarms in accordance with standard operating procedures.
  • Perform required specific testing and operate specified laboratory equipment, as applicable.
  • Perform environmental monitoring and clean and disinfect cleanroom suites, as applicable.
  • Perform other duties as assigned.

About the Company

NAMSA

MedTech CRO delivering end-to-end device development

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.

Company size
1,001-5,000
Company stage
Not listed
Total funding
Not listed
Headquarters
Toledo, OH
Founded
1967

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