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...

This person will be a Regulatory liaison between product development and the regulatory agencies. Experience with eCTD filings; Regulatory Affairs Certification (RAC). Regulatory support in drug listi...

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...

Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and HQ colleagues regarding labeling compliance to accomplish company goals. This individual works cross-functionally with internal ...

Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...

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...

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...

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 ...

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

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...

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 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...

Eligibilities & qualifications.

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

Determine appropriate regulatory requirements and strategies for new product development projects including both domestic and foreign activities and provide regulatory consultation to other internal a...

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...