Regulatory Documentation Jobs (NOW HIRING)

Regulatory Documentation Specialist Location: Maplewood, MN Expected Duration: 6 months Kickstart or grow your career in global regulatory affairs! Join a fast-paced, collaborative environment where ...

The role reports to the Regulatory and Documentation Advisory team and offers the opportunity to collaborate across multiple functions to deliver thoughtful, client-focused solutions in a dynamic ...

Position Summary The Specialist II, Regulatory Documentation reports to the Director, Regulatory Documentation and will provide support in the management and publishing of documents ensuring its ...

Position Summary The Specialist III, Regulatory Documentation will report to the Director, Regulatory Documentation and will provide expertise and guidance in the management and publishing of ...

The role reports to the Regulatory and Documentation Advisory team and offers the opportunity to collaborate across multiple functions to deliver thoughtful, client-focused solutions in a dynamic ...

Applies regulatory documentation standards that enhance efficiency and ensure consistency across the entire development and life cycle management of TA assets, across geographic regions. Leads ...

Applies regulatory documentation standards that enhance efficiency and ensure consistency across the entire development and life cycle management of TA assets, across geographic regions. Leads ...

Experience with large regulatory documents is a plus, but it is not a requirement. The ideal candidate has 5+ years experience with regulatory workflows. In order to meet deadlines, the candidate may ...

Prepare, review, and submit regulatory documentation for clinical trial applications, product registrations, and approvals in compliance with relevant regulations (e.g., FDA, EMA). * Coordinate and ...

The Regulatory Affairs Specialist will be responsible for regulatory documentation, compliance, requirements, submissions, and overall regulatory affairs activities. Qualifications * Regulatory ...

Coordinate and maintain regulatory documentation and records for cosmetic products, including ingredient information and compliance certifications. * Collaborate with cosmetic chemistry and product ...

The person will support the compilation, tracking, and processing of regulatory documentation (e.g., affiliate requests, technical documentation, regulatory submissions). * This individual will, also ...

Coordinate and maintain regulatory documentation and records for cosmetic products, including ingredient information and compliance certifications. * Collaborate with cosmetic chemistry and product ...

Managing certification documentation and coordinating plant walkthroughs and audits with QA teams. * Monitor regulatory activities and plant compliance with regulatory safety standards and act as a ...

Maintain and update regulatory documentation for Class I medical devices; support Class II documentation where applicable. * Assist with Design History Files, Device Master Records, Technical Files ...

Managing certification documentation and coordinating plant walkthroughs and audits with QA teams. * Monitor regulatory activities and plant compliance with regulatory safety standards and act as a ...

Managing certification documentation and coordinating plant walkthroughs and audits with QA teams. * Monitor regulatory activities and plant compliance with regulatory safety standards and act as a ...

Managing certification documentation and coordinating plant walkthroughs and audits with QA teams. * Monitor regulatory activities and plant compliance with regulatory safety standards and act as a ...

This position focus on submitted documents preparing, helping to secure timely product approvals and regulatory clearances. Key Responsibilities * Prepare, review, and coordinate the submission of ...

This position focus on submitted documents preparing, helping to secure timely product approvals and regulatory clearances. Key Responsibilities * Prepare, review, and coordinate the submission of ...