This individual works cross-functionally with internal and external departments on Regulatory Affairs labeling related issues. Effective collaboration with Regulatory Affairs, CMR, Supply Chain, and H...

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...

Conceive of and Implement the Regulatory Strategy in collaboration with Cross-Functional (Solution Leaders, SBU Marketing, Medical Affairs, BU Regulatory and other) partners. The Principal Regulatory ...

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...

Experience with eCTD filings; Regulatory Affairs Certification (RAC). This person will be a Regulatory liaison between product development and the regulatory agencies. Manage all Regulatory, Federal a...

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 ...

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...

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...

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. Keeps abreast of ...

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...

Support daily Regulatory Affairs function eg; compliance to CFR ,, ISO requirements, Company policies, operating procedures, processes, promotional task assignments into windchill and assigned trainin...

Eligibilities & qualifications.

Analyzes and communicate the adequacy of proposed regulatory pathways and strategy for initial product designs and recommend changes or refinements based on initial regulatory outcomes. Applicants wit...