Regulatory specialist jobs in Clifton, NJ
Regulatory Affairs Specialist- (Quality, Regulatory)
Reports to. Manager of Regulatory Affairs Responsibilities. Assist the Manager of Regulatory Affairs.. Generate Raw Material Regulatory statement. Origin Statement, Cruelty Free statement, Heavy metal..
Regulatory Compliance Specialist
Product Stewardship Specialist Lyndhurst, NJ, USA Company Description With over 100 years of experience.. Job Description Product Regulatory expert for Construction Chemical Company responsible for preparing..
Food Regulatory Labeling Specialist
GGG is seeking a detail oriented and self motivated Food Regulatory Labeling professional to join our team in the Paramus, NJ office. In this role, you will be responsible for meeting project..
Regulatory Affairs Specialist
Job Description Job Description. Job Summary. The Regulatory Affairs Specialist is responsible for all.. The role assists the Regulatory Manager and other associates within the Regulatory Department and works..
Regulatory Specialist - Health Active Ingredients - Remote
Your role We are seeking a dynamic and experienced Innovation Regulatory Specialist interested in.. Regulatory Educationo Educate internal teams, including innovation teams, categories, and sales..
Manager, Regulatory Affairs
Works with project management, development, and commercial teams and leads regulatory activities.. Ensures that regulatory files and data systems are maintained and in compliance with related work..
Senior Regulatory Associate
Senior Regulatory Associate. Hybrid, NJ (2 3 days a week) I am currently partnered with a global.. In this role, you will be the Regulatory lead for submission planning and strategy for development..
Regulatory Affairs Manager
The role will be focused on providing CMC regulatory strategy input and expertise around.. Determine regulatory and scientific technical requirements for CMC and GMP related submissions and..
Junior Regulatory Associate
Job Description We are looking for a Junior Regulatory Associate to join our expanding team.. Be responsible for the review and finalization of Global Regulatory Strategy Documents, CTD sections for..
Senior Compliance and Regulatory Specialist
Job DescriptionThe Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global.. Participate in global supplier and regulatory meetings and effectively represent the site. Review and..
Corporate and Regulatory Affairs Specialist
Description templates and other group health plan documents.Perform additional tasks and lead additional work streams, from time to time and upon request, concerning the regulatory regime or..
Senior Regulatory & Compliance Specialist
Friday, 8 00AM. 5 00PMCatalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and.. The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations..
Sr Compliance and Regulatory Specialist
JDThe Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations.. Supplier Quality, Regulatory Compliance, DEA, and QMS.SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES..
Regulatory Affairs Manager (CMC)
Our client is seeking an experienced Regulatory Affairs professional to join their team based in North.. The Regulatory Affairs Manager will be responsible for ensuring compliance with all regulatory standards..
Associate Director Regulatory Affairs
The Associate Director Regulatory Affairs is an integral part of our Regulatory Affairs team based out.. The Associate Director Director plays a key role in developing and executing regulatory strategies and..
Global Regulatory Lead, Oncology, Global Regulatory Strategy & Policy
Pay rate range. 45 55 hr. Position Summary. Objective. Develop global regulatory strategy for Oncology.. remote in the US. Responsibilities. Develop global or US regulatory strategy for Oncology products in..
Global Regulatory Lead, Oncology, Global Regulatory Strategy & Policy
If you've got the expertise, we've got the job! Job Title. Global Regulatory Lead, Oncology, Global.. Remote. Duration. 6 months Position Summary. Objective Develop global regulatory strategy for Oncology..