Job Summary
Job Description
Under limited supervision, the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obt...

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...

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 ...

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...

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 ...

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...

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...

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 ...

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...

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 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...

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 ...

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...

Hiring - Senior Regulatory Affairs Specialist. Support marketing, R&D and Lonza BU in ad hoc projects, in relation to market growth and innovation initiatives by preparing US regulatory assessments fo...

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. They engage in...