Senior Finance Analyst, Core Diagnostics R&D and Regulatory Affairs - Lake Forest, IL

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 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 ...

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

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products. · Prepare and manage U.S. and global regulatory submissions. · Support execution of global regulatory strategies. · ...

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 ...

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. · ...

We are seeking a Regulatory Affairs Associate to support U.S. and global regulatory submissions for medical device products. · Prepare and manage U.S. and global regulatory submissions, including FDA and CE technical documentationCollaborate with R&D and global/regional RA partne ...

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 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 ...

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

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 ...

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 · ...

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

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. · ...

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 ...

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. · ...

The position of Regulatory Affairs Specialist involves managing activities for marketed product variations including authoring and compilation of chemistry, manufacturing, and control sections to ensure timely preparation of submission documents. · ...

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. · ...