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NAMSA

MedTech CRO delivering end-to-end device development

Lab Technologist - In Vitro

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

About the Job

Requirements

  • A bachelor's degree in a scientific discipline appropriate for the hiring department and at least two years of related laboratory experience, or a high school diploma with at least six years of relevant laboratory experience.
  • Awareness of guidelines and regulations applicable to the primary department, potentially including USP, ISO, CTFA, FSA, ICH, EP, and/or JP.
  • Knowledge of the metric system, scientific applications, experimental design, and data evaluation.
  • Ability to draft technical documents and communications, including standard operating procedures, protocols, and Trackwise records.
  • Proficiency with applicable NAMSA systems, such as LIMS, Trackwise, and MasterControl, as appropriate for the primary department.
  • Ability to work in a GMP/GLP environment.
  • Ability to perform the physical activities and meet the vision requirements described, including lifting requirements and working around sharps, blood, and hazardous or caustic chemicals; safety glasses and hearing protection are required in designated areas and for specific tasks.

Responsibilities

  • Prepare test articles or products according to work instructions and execute routine testing under NAMSA standard operating procedures, including appropriate data analysis.
  • Perform routine calculations, interpret results, and escalate positive results or unusual testing occurrences to management.
  • Provide on-the-job training as needed.
  • Ensure testing and test-article preparation meet due dates.
  • Prepare and maintain cell lines and reagents required for testing, as applicable to the primary department.
  • Maintain supplies, materials, equipment, and ancillary records such as logbooks and worksheets used in routine testing.
  • Conduct routine studies independently and, when requested, conduct more involved studies.
  • Participate in improving documents, test systems, quality systems, and workflow.
  • Check laboratory equipment, be on call, and respond to continuous-monitoring alarms according to standard operating procedures, as required.
  • Perform environmental monitoring and clean and disinfect cleanroom suites, as required.
  • Order or stock supplies subject to approval, as required.
  • Perform personal-gowning environmental testing and submit organisms from gowning, environmental, and sterility-test positives for identification and inclusion in monthly trending data, as required.
  • Review incoming test articles and paperwork for appropriateness and accuracy, and raise concerns to management.
  • Operate an autoclave, as required.

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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