Provide input on worldwide regulatory requirements and standards to development teams and ensure that requirements are incorporated in product development. Review and approve product labeling and prom...

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...

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...

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...

Works with personnel in other departments including Marketing, CMR, Legal, and counterparts in NNAS Regulatory Affairs. Maintain up-to-date knowledge of data requirements and formats, applicable curre...

Mario Badescu Skin Care through balanced compliance and will manage all aspects of regulatory activities necessary to maintain and grow our business. Provide regulatory support for new product registr...

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...

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...

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...

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...

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...

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 ...

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...

The Regulatory Affairs Specialist coordinates, facilitates, and reports on post-market regulatory programs. Implements regulatory activities such as obtaining global regulatory clearances and/or appro...

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...

Prepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both dom...

Regulatory expert support IVDR teams, implements regulatory strategies for IVDR activities; provides regulatory leadership; collaborates with the regulatory staff from other business units, companies,...