Regulatory Affairs Specialist - Winnetka - Medline Industries - Transportation & Operations

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 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. · ...

דף הבית » משרות » Regulatory Affairs Specialist · Regulatory Affairs Specialist · מיקום: · יקנעם · אופן העסקה: · היברידי · תיאור התפקיד: · תפקיד הכולל אחריות על ניהול והובלת תהליכים רגולטוריים גלובליים, כולל הכנת מסמכים, הגשות לרשויות, ותמיכה בעמידה בדרישות התקינה והמדיניות הבינל ...

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. · ...

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.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. · ...

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. · ...

This is a 6 months contract position as Regulatory Affairs Specialist. The role involves providing technical information, evaluating regulatory compliance, and supporting risk assessment activities. · ...

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 ...

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. · ...

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 ...

Department · PSD Applied Data Science: Instructional Services and Innovation · About The Department · The Master's in Applied Data Science program (MS-ADS) is a professional graduate program within the Physical Sciences Division (PSD) and the Data Science Institute (DSI) at The U ...

We are seeking a · Regulatory Affairs Specialist · to support regulatory submissions, · global registrations, · labeling reviews, · and compliance activities for Class II/III medical devices. · ...

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 ...

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. · ...

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 ...