| Job alert | Jobs 1 - 10 of 633 |
Director of Regulatory Affairs (FDA)
KMR Search Group
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Jersey City, NJ
... Plan, coordinate, author, and review any submissions to FDA to ensure company requirements and relevant FDA requirements are met. Liaise with Project Managers and participate on global client project teams to properly plan for and support client ... - Jun 04
Supervisor, QC Microbiology
Minaris Regenerative Medicine
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Allendale, NJ, 07401
... Strong knowledge of FDA and EU regulatory standards. cGMP experience required. Strong knowledge of microbiological test methods and philosophies. Strong knowledge of quality systems and ability to interpret Quality standards of implementation and ... - Jun 05
R&D Manager
Joulé
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Montvale, NJ, 07645
... Provide oversight and direction for individuals and teams responsible for: creating and executing R&D programs and initiatives Expert knowledge and strong experience in FDA regulated environment, specifically OTC drugs (NDA and Monographed) as well ... - Jun 04
R&D Manager
Joulé
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Montvale, NJ, 07645
... Provide oversight and direction for individuals and teams responsible for: creating and executing R&D programs and initiatives Expert knowledge and strong experience in FDA regulated environment, specifically OTC drugs (NDA and Monographed) as well ... - Jun 04
Senior Facilities Technician
Minaris Regenerative Medicine
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Allendale, NJ, 07401
... Ensure compliance to all FDA and Worldwide Quality & Compliance regulations (As applicable to the job function). Attend all required Quality & Compliance training at the specified interval. Minimum Required Training to be Completed within the First ... - Jun 01
Staff Regulatory Compliance Specialist (Hybrid)
Stryker Corporation
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Mahwah, NJ, 07430
... You will perform recall activities including facilitating technical and medical assessments, completing product field action assessments, sending recall communications to the field, and gathering and submitting relevant documents to FDA. * Address ... - May 21
Manager, Global Regulatory Affairs, Marketed Products
Takeda Pharmaceutical
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Clifton, NJ, 07015
... Regulatory submissions to US FDA, EU, Health Canada, and other international health authorities – Support regulatory team and Global Regulatory Lead (GRL) in preparations and timely delivery of detailed and accurate regulatory submissions for drugs, ... - Jun 03
Lead QC Microbiology Engineer
Minaris Regenerative Medicine
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Allendale, NJ, 07401
... Comprehensive knowledge of regulatory requirements and standards (FDA, EU, ICH, ISO, USP) Proficient with method verification/method transfer and equipment/instrument validation. Maintain current awareness and contribute to current scientific ... - Jun 05
Quality Assurance Engineer
10XBeta Venture Studio
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Manhattan, NY, 10261
... Preferred: ● Working knowledge of ISO 13485, ISO 14971, 21 CFR 820, IEC 60601-1, IEC 62304, FDA’s General Principles of Software Validation. ● Passion for the development and execution of new technologies, including the ability to apply and manage ... - May 17
Quality Assurance Manager for Pharmaceutical Packaging
Carecam International Inc
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Fairfield, NJ
... The Quality Assurance Manager will ensure compliance with current Good Manufacturing Practices (cGMP) as they pertain to the local regulation and exporting countries regulation as applicable (such as FDA, MHRA, EMA, Health Canada). Overall ... - Jun 02