Enhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
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. You will work closely with cross-functional teams to support product development, manufacturing, and...
read moreWe 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 ...
read moreThis 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...
read moreProvide regulatory support to the internal R&D team and external customers. Must be able to prioritize and provide input on regulatory aspects. This individual provides support to internal and externa...
read morePrincipal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist.
Senior Regulatory Affairs Specialist. Senior Regulatory Affairs Specialist. The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation update...
read moreEnhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
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...
read moreEnhance your skills in regulatory affairs and documentation management. Investigate, maintain, and manage regulatory product certification claims data, databases, and documentation systems.
The Senior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of reviewers. Senior Regulatory Affairs Spe...
read moreCompany & 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...
read morePrincipal Regulatory Affairs Specialist page is loaded. Principal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist.
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...
read moreCompany & 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...
read moreIn alignment with responsible Regulatory Affairs Management, the Senior Regulatory Affairs Specialist, (Advertising/Promotion) is responsible for reviewing, editing and supporting compliance of SWMI a...
read morePrincipal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist. Defines regulatory strategies and performs regulatory assessments.
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...
read morePrincipal Regulatory Affairs Specialist. Principal Regulatory Affairs Specialist. Follows scientific arguments, identifies regulatory scientific data needs, and solves regulatory issues.
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...
read moreThe 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...
read moreSenior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of reviewers. Senior Regulatory Affairs Special...
read moreThe 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...
read moreSenior Regulatory Affairs Specialist will be responsible for coordination of Performance Evaluation documentation updates within a cross-functional team of reviewers. Senior Regulatory Affairs Special...
read moreWe 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 ...
read moreWe 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 ...
read moreAlliedTravelCareers 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...
read moreAlliedTravelCareers 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...
read moreAlliedTravelCareers 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...
read moreAlliedTravelCareers 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...
read moreEnsure care, safety and cleanliness standards are met according to regulatory compliance.
Prepares robust regulatory applications (either for FDA or for international regulatory agencies) to achieve departmental and organizational objectives. Acts as core team member providing review and a...
read moreActs as core team member providing review and analysis of applicable regulatory guidelines and project regulatory assessments as needed. Prepares robust regulatory applications (either for FDA or for ...
read moreWhich 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...
read moreWhich 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...
read moreTitle: Regulatory Affairs Ops Specialist I. Managing the preparation of regulatory submissions for IND, ANDA, NDA, K, Clientrom, and other electronic submission types. Creating timelines for regulator...
read moreTitle: 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 II. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication o...
read moreTitle: Regulatory Affairs Ops Specialist II. Responsible for the implementation of complex global regulatory strategies, obtain and maintain marketing authorizations for product(s) and communication o...
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