Regulatory Affairs Associate - Florham Park
1 month ago

Job summary
We are seeking a Regulatory Site Quality Specialist to support a leading CPG company's OTC drug listing portfolio.This role will manage the drug listing process for skincare and cosmetic products, ensuring compliance with FDA regulations and GMP standards.
Job description
, consectetur adipiscing elit. Nullam tempor vestibulum ex, eget consequat quam pellentesque vel. Etiam congue sed elit nec elementum. Morbi diam metus, rutrum id eleifend ac, porta in lectus. Sed scelerisque a augue et ornare.
Donec lacinia nisi nec odio ultricies imperdiet.
Morbi a dolor dignissim, tristique enim et, semper lacus. Morbi laoreet sollicitudin justo eget eleifend. Donec felis augue, accumsan in dapibus a, mattis sed ligula.
Vestibulum at aliquet erat. Curabitur rhoncus urna vitae quam suscipit
, at pulvinar turpis lacinia. Mauris magna sem, dignissim finibus fermentum ac, placerat at ex. Pellentesque aliquet, lorem pulvinar mollis ornare, orci turpis fermentum urna, non ullamcorper ligula enim a ante. Duis dolor est, consectetur ut sapien lacinia, tempor condimentum purus.
Access all high-level positions and get the job of your dreams.
Similar jobs
The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Associate Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. ...
1 month ago
The Associate is responsible for managing low to medium impact submission projects and ensuring the timely delivery of high-quality dossiers. The role involves establishing and maintaining submission content planners and timelines, · facilitating tactical team meetings, · prepari ...
1 month ago
The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submiss ...
1 month ago
The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Associate, Regulatory Affairs Submission Management, manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submis ...
1 month ago
The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams.This individual establishes and maintains submission content planners and associated timelines, facilitates tac ...
1 month ago
The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Regulatory Affairs Associate supports regulatory submission management activities for development marketing and post-marketing applications. This role manages low to medium complexity submission projects coordinates cross-functional teams and ensures timely delivery of high-q ...
1 month ago
Join a dynamic team dedicated to seamless execution of global regulatory submissions. · ...
1 month ago
We seek a · Regulatory Site Quality Specialist · to support a leading CPG company's OTC drug listing portfolio. · ...
1 month ago
The Regulatory Affairs Associate I manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Regulatory Affairs Submission Management team manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · This individual establishes and maintains submission content planners and associated timelines, facilitates tactic ...
1 month ago
Manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Regulatory Affairs Associate I - Submission Management supports regulatory submission activities by managing low- to medium-impact regulatory submission projects. · This role is responsible for coordinating submission content, maintaining submission timelines, supporting publ ...
1 month ago
The Associate Director, Regulatory Affairs US Advertising and Promotion is responsible for setting strategy and leading cross-functional, multidisciplinary, therapeutic teams, · ...
1 week ago
The Regulatory Affairs Associate I manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · ...
1 month ago
The Associate, Regulatory Affairs Submission Management manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · Manages low to medium impact (with respect to internal visibility, risk, complexity and criticality) submiss ...
1 month ago
The Regulatory Affairs Associate manages low to medium impact submission projects involving multiple cross-functional regulatory submission teams. · With input from the submission teams this individual establishes and maintains submission content planners and associated timelines ...
1 month ago
The Associate manages submission projects involving multiple cross-functional regulatory submission teams. · Responsibilities · Acts as RA Submissions support providing guidance and communication of established submission processes. · ...
1 month ago