We are seeking a Regulatory Affairs Specialist to provide regulatory support and expertise for U.S. and global medical device submissions. · Provide regulatory support for U.S. and global submissions, including analysis of requirements and tracking deliverablesAssist with executi ...

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products.This role will assist in executing global regulatory strategies, · preparing and maintaining registration dossiers, · and ensuring compliance with FDA,EU,an ...

We are seeking an experienced Regulatory Affairs Associate II to join our team. The successful candidate will have direct medical device regulatory experience with recent hands-on EU MDR 2017/745 experience. · ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

The job is to work as a Regulatory Affairs Associate II in Lake Forest, IL 60045 for 12 months. The job requires a Bachelor's Degree preferably in pharmacy or related subject and RAC Certification. · Proven strong understanding of FDA and worldwide submission requirements. · Prep ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

Provide regulatory support and expertise associated with US and global submission requirements. · ...

We are seeking a Regulatory Affairs Associate to join one of our leading healthcare clients. · ...

The Regulatory Affairs Associate I supports regulatory submission activities for marketed pharmaceutical products. · The position requires strong coordination skills and attention to detail. ...

+Provide regulatory support and expertise associated with US and global submission requirements. · +Drives projects forward and executes agreed upon strategies. · Plans registration packages for device products. · ...

The Regulatory Affairs Associate will be responsible for managing and compiling regulatory submissions for marketed product variations. · Manage, compile, and author CMC sections for marketed product variations · Partner with RA CMC Project Leads to develop Module 3 content · ...

We are hiring Regulatory Affairs Associate II for one of our clients. · Provide regulatory support and expertise associated with US and global submission requirements. · ...

The Regulatory Affairs Associate I supports regulatory submission activities for marketed pharmaceutical products. · Author, compile, and manage CMC sections (CTD Module 3) for marketed product variations. · Ensure regulatory documents meet structural, formatting, and content req ...

This role provides regulatory support and guidance associated with global and US registration of device products. · Drives projects forward and executes agreed upon strategies and plans with oversight. · Maintains awareness of applicable regulations. · Plans and organizes registr ...

We are hiring Regulatory Affairs Associate II for one of our clients. The position will provide regulatory support and expertise associated with US and global submission requirements. · Drives projects forward and executes agreed upon strategies and plans with oversight. · ...

This position will coordinate activities with all functional departments in support of regulatory filings. · Manage and compile CMC sections of marketed product variations. · Partner with RA CMC Project Leads and develop module 3 content and project timelines. · ...

This role is responsible for managing, authorizing and compiling Chemistry, Manufacturing and Controls (CMC) documentation for marketed product variations and regulatory submissions. The position partners closely with cross-functional teams to ensure CMC sections meet regulatory ...

Provides regulatory support and guidance associated with global and US registration of device products. Assures full regulatory compliance of all documentation for submissions and change management. · Drives projects forward and executes agreed upon strategies and plans with over ...

Job summaryThe Associate II provides regulatory support and guidance associated with global and US registration of device products. · Maintains awareness of applicable regulations. · Evaluates manufacturing and labeling changes for regulatory impact. · ...

The Sr. · Regulatory Affairs Manager, · hired in this role will work out of the · Lake Forest, IL (or ourTown Center, San Diego, CA) · , location 4-5 days a week in the office. This role will require some travel up to 25% to Abbott locations potentially in and outside of the US.T ...

The Regulatory Affairs Associate I supports regulatory activities for marketed products with a focus on chemistry manufacturing and control documentation. · ...