NAMSA
1001 - 5000 employees
Founded 1967
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare Insurance • Biotechnology • Pharmaceuticals
NAMSA is a global leader in medical device testing and research, offering comprehensive consulting, preclinical research, clinical research, and testing services for medical device and IVD manufacturers worldwide. With a team of over 1,400 specialists and state-of-the-art labs across North America, Europe, and Asia, NAMSA conducts extensive testing to ensure the safety, efficacy, and compliance of medical devices. The company provides strategic consulting on regulatory submissions and market strategies, helping clients navigate complex regulatory landscapes efficiently and effectively. Founded in 1967, NAMSA is trusted by manufacturers to deliver high-quality services from concept to commercialization.
Biological Safety Specialist
🔥 9 minutes ago
🗣️🇫🇷 French Required
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NAMSA
1001 - 5000 employees
Founded 1967
⚕️ Healthcare Insurance
🧬 Biotechnology
💊 Pharmaceuticals
Healthcare Insurance • Biotechnology • Pharmaceuticals
NAMSA is a global leader in medical device testing and research, offering comprehensive consulting, preclinical research, clinical research, and testing services for medical device and IVD manufacturers worldwide. With a team of over 1,400 specialists and state-of-the-art labs across North America, Europe, and Asia, NAMSA conducts extensive testing to ensure the safety, efficacy, and compliance of medical devices. The company provides strategic consulting on regulatory submissions and market strategies, helping clients navigate complex regulatory landscapes efficiently and effectively. Founded in 1967, NAMSA is trusted by manufacturers to deliver high-quality services from concept to commercialization.
📋 Description
• Develop and maintain biological safety documents and reports • Assess/audit compliance of biocompatibility and material characterization results to applicable standards • Collaborate with teams for regulatory compliance and safety standards
🎯 Requirements
• Bachelor’s degree or equivalent experience in a related field • Master’s or Doctorate degree or equivalent experience in a related field, and a minimum of 2 years of relevant experience. • 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
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