Regulatory Documentation Jobs (NOW HIRING)

We are currently seeking ​a Regulatory Documentation Clerk to join our team! You will be responsible for the preparation of regulatory documents required to be issued with products sales. Clerk ...

We are currently seeking a Regulatory Documentation Clerk to join our team! You will be responsible for the preparation of regulatory documents required to be issued with products sales. Clerk will ...

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 ...

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 ...

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 ...

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 ...

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 ...

The position focuses on managing regulatory documentation, facilitating IRB submissions, and ensuring that all regulatory requirements for clinical studies are met in a timely and accurate manner.

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 role executes defined regulatory strategies, facilitates documentation exchange with manufacturing sites and franchise partners, and ensures submissions are complete, accurate, and aligned with ...

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 ...

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

Coordinate regulatory documentation, certifications, and compliance data. * Manage tender timelines, trackers, KPIs, and project deliverables. * Identify risks and implement mitigation strategies to ...

Document Preparation & Submission: Assist in preparing and submitting regulatory documents to IRBs, sponsors, and internal stakeholders including initial submissions, amendments, continuing reviews ...

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

The Regulatory Affairs Specialist Assistant supports the regulatory operations of the clinical ... Track document expirations and ensure timely updates (licenses, GCP training, certifications ...

Coding of administrative and regulatory documents. * Verification of documentation, maintenance of document tracking system. * Collaborating with CTM to determine to issues in regulatory ...