Regulatory Affairs Specialist - Glenview, Illinois, United States

The Stefanini Group is hiring a Regulatory Affairs Specialist to work within an Export Regulatory and Quality team. · Reviewing nutrition and regulatory compliance · ...

This role will work within an Export Regulatory and Quality team reviewing nutrition and regulatory compliance and providing support in the Quality area related to Client products globally. · ...

This role will work within an Export Regulatory and Quality team reviewing nutrition and regulatory compliance providing support in the Quality area related to Client products globally. · ...

This role will work within an Export Regulatory and Quality team.This position will be responsible for reviewing nutrition and regulatory compliance and providing support in the Quality area related to Client products globally. · ...

Stefanini Group is hiring Regulatory Affairs Specialists in Glenview. · The ideal candidate will possess a B.S. in Food Science or related scientific field with minimal experience in Regulatory, Nutrition, R&D or Quality required.This position requires the ability to handle compl ...

This role will work within an Export Regulatory and Quality team.This position will be responsible for reviewing nutrition and regulatory compliance and providing support in the Quality area related to Client products globally. · ...

The Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. · ...

Under general supervision the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. · ...

Under general supervision the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals Prepare comprehensive regulatory strategies for new devices new launch markets and post-market d ...

Under general supervision works to ensure products and processes meet all applicable state federal local regulations and industry best practices for distribution of regulated products food pharmaceuticals or medical devices. · ...

Under general supervision, the Regulatory Specialist is responsible for planning and executing global regulatory activities necessary to obtain and maintain global regulatory approvals. · Prepare comprehensive regulatory strategies for new devices, new launch markets, and post-ma ...

Under limited supervision the Senior Regulatory Specialist is responsible for planning and executing critical and complex global regulatory projects necessary to obtain and maintain global regulatory approvals. · ...

The Regulatory Specialist will prepare, amend, and maintain product registration dossiers for all product categories within Milk Quality and Animal Health. The role involves working closely with regulatory colleagues across multiple departments. · Responsible for product registra ...

This job provides information and guidance to students and others regarding the Department of Veterans Affairs educational benefits. The specialist assists with various job duties related to financial aid. · ...

We are seeking an individual that is dedicated and motivated with the ability to make decisions as Regulatory Specialist responsible for preparing dossiers for product registrations in North America. · Responsible for state and federal preparation submissions and maintenance of e ...

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 Specialist · to support regulatory submissions, · global registrations, · labeling reviews, · and compliance activities for Class II/III medical devices. · ...

The Medical Affairs Specialist researches and develops documents that support the safety and efficacy of products. · They lead research activities for assigned projects critically evaluating and interpretating scientific data and communicating data impact to assigned products and ...

The Medical Affairs Specialist contributes to integrated medical plans, evidence generation, regulatory submissions, and scientific communications for pharmaceutical and medical device products. · ...

The Medical Affairs Specialist researches and develops documents that support the safety and efficacy of products. They critically evaluate scientific data and communicate its impact to assigned projects. · ...