Regulatory Associate - Streamwood

The Regulatory Associate supports the team in managing the product lifecycle management system. Ensures compliance with emerging regulations and demonstrates proficiency in Genesis ESHA labeling software system. · Ensure the product lifecycle system is up to date. · Create and up ...

The Regulatory Associate is responsible for supporting the team in managing the product lifecycle management system.This includes creating specifications and verifying supplier documents, managing customer information requests, · developing nutritional fact labels, · y ensuring c ...

The Regulatory Associate is responsible for supporting the team in managing the product lifecycle management system. · This includes creating specifications and verifying supplier documents, managing customer information requests, developing nutritional fact labels, and ensuring ...

The Regulatory Associate is responsible for supporting the team in managing the product lifecycle management system.This includes creating specifications and verifying supplier documents, managing customer information requests, developing nutritional fact labels, and ensuring com ...

The Regulatory Associate is responsible for supporting the team in managing the product lifecycle management system.This includes creating specifications and verifying supplier documents, managing customer information requests, · developing nutritional fact labels, · and ensuring ...

We're seeking a detail-oriented Regulatory Associate who's passionate about the food industry and ready to play a key role in ensuring our products meet the highest regulatory and customer standards. · ...

+h2>Job summary · The Regulatory Associate supports the team in managing product lifecycle management systems. · +Ensure product lifecycle system is up-to-date. · Create and update specifications for new product rollouts. · Support change management process. · +Bachelor's degree ...

We are seeking a detail-oriented Regulatory Associate who's passionate about the food industry and ready to play a key role in ensuring our products meet the highest regulatory and customer standards. · Ensure the product lifecycle system is up to date. · Create and update specif ...

Ready to launch your career in Regulatory Affairs? Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, gro ...

+Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, growth, · and making an impact in a global industry. ...

Join our collaborative team dedicated to quality and innovation in dental medical devices. You'll gain hands-on experience in product registration and compliance while working in a supportive environment that values learning, growth, and making an impact in a global industry. · ...

Join a team where your expertise drives product integrity, innovation, and compliance. We're seeking a detail-oriented Regulatory Associate who's passionate about the food industry and ready to play a key role in ensuring our products meet the highest regulatory and customer stan ...

We are looking to add an · Affiliate to our Energy practice group's regulatory team Please note that Illinois experience is required. ...

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 ...

Responsible for technical writing of files in accordance with In Vitro Diagnostic medical device Regulation (IVDR) and provides regulatory support for diagnostic product development and commercial diagnostic products. · ...

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. · ...

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. · ...

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 · ...