97 Iso Jobs in Brooklyn, NY
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Research and Development Engineer I/II - Process Development Cresilon, Inc. - Brooklyn, New York Manufacturing Practices (cGMP) requirements. Work experience with the medical device or pharmaceutical industries preferred Working knowledge of ISO 9001, ISO 13485:2003 and ISO 14971:2007 preferred. Working 8 days ago
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Manager Process Engineering (Chemical Process / Med Device Manufacturing) Cresilon, Inc. - Brooklyn, New York providers. Strong knowledge of medical device regulations (e.g., 21 CFR Part 820), cGMP, and related standards (e.g., ISO 13485) is preferred. Strong project management and organizational skills, including 8 days ago
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Medical Device R&D Project Leader Cresilon, Inc. - Brooklyn, NY ) Certification is strongly preferred. Formal training and experience in developing and commercializing regulated devices under Design Control (21 CFR 820) requirements, GLP/GMP, and ISO regulations is required 100,000 - 160,000 9 days ago
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Medical Device R&D Project Leader Cresilon, Inc. - Brooklyn, New York ) Certification is strongly preferred. Formal training and experience in developing and commercializing regulated devices under Design Control (21 CFR 820) requirements, GLP/GMP, and ISO regulations is required 8 days ago
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Senior Quality Control Chemist Cresilon, Inc. - Brooklyn, New York Proficiency: • Applicable cGMP medical device requirements from USA 21 CFR § 820 and ISO 13485 • Physical characterization methods and physical method validation • Laboratory Information Management Systems 22 days ago
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Research and Development Medical Device Engineer Cresilon, Inc. - Brooklyn, NY disclosures. Ensuring that all design activities adhere to FDA Quality System Regulations and ISO 13485 design control and risk management requirements. Lead material/design/process changes through a design 60,000 - 160,000 More than 30 days ago
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Associate Production Engineer Cresilon, Inc. - Brooklyn, New York observations Preferred Qualifications: · Master’s Degree with a background in Mechanical or Chemical Engineering · Experience in GMP, ISO, and FDA regulated environments · Cleanroom experience (ISO Class 5 to 8 24 days ago
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Compliance Specialist Cresilon, Inc. - Brooklyn, New York The Compliance Specialist provides guidance and ensures compliance with ISO13485 & 21 CFR Part 820 and applicable good manufacturing practice regulations within the company. Also provides support 26 days ago
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Quality Assurance Manager AP Rochester - , NY, United States the team and facilities supporting metal finishing processes, ensuring compliance with AS9100D, ISO 9001:2015, and Nadcap quality management systems. RESPONSIBILITIES Oversee all quality functions, including 7 days ago
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Research and Development Medical Device Engineer Cresilon, Inc. - Brooklyn, New York disclosures. Ensuring that all design activities adhere to FDA Quality System Regulations and ISO 13485 design control and risk management requirements. Lead material/design/process changes through a design More than 30 days ago
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