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Regulatory Affairs Specialist Jobs in Jersey City, New Jersey

7 jobs

Review and approve raw materials and ingredient information submitted globally in accordance with regulations for both industry and international guidelines. Review and ensure product primary/secondary labeling requirement compliance Maintain and apply working knowledge of changing global regulations, regulatory standards and protocols to ensure compliance with various domestic & international g...
Review and approve raw materials and ingredient information submitted globally in accordance with regulations for both industry and international guidelines. Review and ensure product primary/secondary labeling requirement compliance Maintain and apply working knowledge of changing global regulations, regulatory standards and protocols to ensure compliance with various domestic & international g...
Our Industry: Where we play We sit at the intersection of technology and Life Sciences industries. Humbly, we’ve been told that we are the leader in application software for the clinical development process, tackling real-world problems and making a real difference in the lives of patients everywhere. With the current transformation in the life sciences industry, we are at the forefront of provid...
Job Title: Regulatory Affairs Specialist Summary: The Regulatory Affairs Specialist (RAS) performs tasks related to study related regulatory documents, IRB submissions, and other site documentation, including quality control of study documentation. The RAS is responsible for developing and maintaining positive relationships with sponsors as well as internal study teams through oral and written co...
Our Industry: Where we play We sit at the intersection of technology and Life Sciences industries. Humbly, we’ve been told that we are the leader in application software for the clinical development process, tackling real-world problems and making a real difference in the lives of patients everywhere. With the current transformation in the life sciences industry, we are at the forefront of provid...
This position reports to the Director of Regulatory Affairs F&N. The individual will be responsible to independently provide Symrise Inc. customers with product safety/regulatory information in accordance with US FDA/FEMA guidelines, customer specific guidelines and various international regulations. In addition, this position may support the TTB filings of Drawback Alcohol and related TTB fu...
Job Description: Quality Assurance Regulatory Affairs Specialist REPORTS TO PRIMARY FUNCTION Quality Assurance Manager Prepare US and International regulatory filings and registrations. Ensure compliance with US and international regulations, standards and guidance. RESPONSIBILITIES Prepare FDA and international submissions for new products and product changes as required to ensure timely approva...