The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...

Experience:Minimum of 5+ years of experience in Regulatory Affairs within the personal care and cosmetics industry and OTC, with a demonstrated track record of Regulatory Compliance and Product regist...

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. This individual works cross-functionally with internal and external departments on Regulatory Af...

Works with personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs. Works with manager to compose letters incorporating NN position on external regu...

Req: Masters in Pharmacy Administration and Regulatory Affairs or rltd + 3 months exp in the use of SOPs.

Our Senior Regulatory Affairs Specialist position is primarily focused on maintaining continued market access of our existing product portfolio, in addition to opportunities to provide regulatory supp...

Regulatory Affairs Project management experience. Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects a...

The Labeling Specialist supports the development of labeling activities for all regulatory submissions. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding ...

Cosmetic or related industry experience, including 5+ years of Regulatory experience. Mario Badescu Skin Care through balanced compliance and will manage all aspects of regulatory activities necessary...

Our client is looking to fill the role of Regulatory Affairs Specialist. The primary responsibility is writing regulatory submissions by successfully coordinating with the Regulatory Consultant and Ma...

Our client is looking to fill the role of Regulatory Affairs Specialist. The primary responsibility is writing regulatory submissions by successfully coordinating with the Regulatory Consultant and Ma...

Coordinates the collection of documents, records, reports, and data from the Development, Clinical Affairs, Quality, and Operations Departments for inclusion in regulatory documents. Responsible for t...

Minimum 1-3 years' experience in Regulatory Affairs in the medical device industry. Provides administrative support for regulatory affairs manager. Conducts regulatory assessments and determines need ...

Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New York State Department of Health, CMS and oth...

The PV Analytics and Reporting Specialist, PV Analytics Center of Excellence contributes to the ongoing development, implementation, and successful execution of the scientific, operational, and regula...

The Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...

Performs quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) ...

Maintains advanced and current knowledge of relevant regulations, policies, and guidelines and acts as Regulatory Affairs Subject Matter Expert in assigned areas. Provides guidance/direction within th...

Working knowledge of relevant federal and state regulatory programs (e.

The Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Assisting in gatherin...