The Senior Regulatory Affairs Specialist will work in BD – Specimen Management providing regulatory leadership to cross-functional project teams from early development to new product launches in vario...

The Principal Regulatory Specialist is responsible for carrying out Pre-Market and Post-Market regulatory activities in compliance with Digital Factory’s Quality Management System for domestic and var...

CMC Regulatory Affairs Specialist performs regulatory assessment of changes, interpreting the current, approved and planned clinical regulatory landscape by contributing to the regulatory submission f...

Develop and maintain procedures and systems to perform regulatory operational activities. Keep abreast of new regulatory changes in all target markets globally and new cosmetic regulations and guideli...

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...

Mario Badescu Skin Care through balanced compliance and will manage all aspects of regulatory activities necessary to maintain and grow our business. Provide input on worldwide regulatory requirements...

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...

The Quality and Regulatory Specialist facilitates and participates in the implementation of the multidisciplinary hospital and system wide Clinical Quality and Patient Safety Performance Improvement P...

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...

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

The main function of a regulatory affairs specialist is to implement policies and coordinate community affairs strategies. A typical regulatory affairs specialist will develop and maintain supportive ...

Experience working on regulatory or governmental matters, directly or in a support role, with state energy regulators or legislators; a diversity of operational or staff position experience working fo...

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...

Certification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Monitor and submit applicable reports and ensure appropriate responses are submitted to regulatory authorities. ...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulat...

Eligibilities & qualifications.

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...

Regulatory Affairs Documentation Specialist. A Regulatory Affairs Documentation Specialist utilizes strong written communication skills to enhance the level of documentation maintained within the Depa...