Job Summary
Under general supervision, the Regulatory Specialist is responsible for planning and executing regulatory activities necessary to bring new Over-the-Counter (OTC) Drugs and Cosmetics to...

Enhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.

We are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Ensure regulatory compliance with global standards and provide timely regulatory advice to internal ...

We are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. You will work closely with cross-functional teams to support product development, manufacturing, and...

Enhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.

Identify regulatory challenges relevant to commercial opportunities and serve as a subject matter expert by collaborating cross-functionally to solve them. Provide regulatory support to the internal R...

This individual provides support to internal and external customers in order to ensure that all domestic and global regulatory requirements and compliance needs are fulfilled according to legal and co...

Principal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist.

Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of re...

The Senior Regulatory Affairs Specialist overseeing advertising and promotional Regulatory responsibilities, works closely and partners with internal departments to efficiently and effectively meet as...

The Senior Regulatory Affairs Specialist combines knowledge of scientific, regulatory and business issues to ensure that advertising and promotion activities meet geography specific regulatory require...

Enhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.

Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of re...

Enhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.

Company & Benefits Information At Blain's Farm & Fleet we believe everyone deserves the opportunity to have a job they love, work in a great environment, grow their career & enjoy a positive balance.A...

Field Marketing Brand Ambassador.Please be advised of the following:.The basic job responsibilities for this role require a vehicle and valid driver's license.Candidates not possessing a reliable vehi...

Principal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist.

Company & Benefits Information At Blain's Farm & Fleet we believe everyone deserves the opportunity to have a job they love, work in a great environment, grow their career & enjoy a positive balance.A...

Gather and analyze the necessary data to ensure compliance with domestic (FEMA GRAS, FDA) and international (Health Canada, JECFA, GCC, Mercosur) regulatory requirements for flavors and finished goods...

Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist. Follows scientific arguments, identifies regulatory scientific data needs, and solves regulatory issues.

Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist. Defines regulatory strategies and performs regulatory assessments.

The position of **Regulatory Affairs Specialist I** is within our Infectious Disease Developed Markets business unit. Prepares and Submits Regulatory Reports for FDA and other OUS (Outside of US) Re...

The position of **Regulatory Affairs Specialist I** is within our Infectious Disease Developed Markets business unit. Prepares and Submits Regulatory Reports for FDA and other OUS (Outside of US) Re...

Gather and analyze the necessary data to ensure compliance with domestic (FEMA GRAS, FDA) and international (Health Canada, JECFA, GCC, Mercosur) regulatory requirements for flavors and finished goods...

Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of reviewers. Senior Regulatory Affairs Special...

Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of reviewers. Senior Regulatory Affairs Special...

We are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. Bachelor's degree in Life Sciences, Engineering, Regulatory Affairs, or a related field. Ensure regu...

We are seeking an experienced Quality Assurance and Regulatory Affairs Specialist to join our team. You will work closely with cross-functional teams to support product development, manufacturing, and...

AlliedTravelCareers is working with Fusion Medical Staffing to find a qualified RRT in Park Ridge, Illinois, 60068!.Fusion Medical Staffing is seeking a skilled Respiratory Therapist for a 13 week tra...

AlliedTravelCareers is working with Triage Staffing LLC to find a qualified Resp Tech in Park Ridge, Illinois, 60068!.Travel Cardiopulmonary: Respiratory Therapy Park Ridge.Shift Details: 12H Nights...

AlliedTravelCareers is working with Fusion Medical Staffing to find a qualified RRT in Park Ridge, Illinois, 60068!.Fusion Medical Staffing is seeking a skilled Respiratory Therapist for a 13 week tra...

Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Reviews and evaluates communications to ensure ...

Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Reviews and evaluates communications to ensure ...

Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as re...

Which includes: tracking of status and progress of regulatory documentation, reviewing, editing and proofreading regulatory documentation, participating as an active team member of project teams as re...

Title: Regulatory Affairs Ops Specialist I. Overseeing authoring and reviewing of regulatory documents. Identifying and assessing regulatory risks and risks to timelines.

Title: Regulatory Affairs Ops Specialist I. Solid understanding and experience and interpretation of regulatory requirements, with particular Client on the US region. Creating timelines for regulatory...

Title: Regulatory Affairs Ops Specialist II. Compile and submit, in a timely manner, regulatory documents according to regulatory requirements. Lead or represent Regulatory Affairs in project teams.

Title: Regulatory Affairs Ops Specialist II. Lead or represent Regulatory Affairs in project teams. Responsible for the implementation of complex global regulatory strategies, obtain and maintain mark...