Regulatory Specialist: salario promedio en New Brunswick, NJ in 2024
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Regulatory Operations Specialists - II (Associate)
Regulatory Operations Specialists - II (Associate). The specialist position also works as part of a team to prepare and submit marketed product reports to the regulatory authorities; maintains US state registrations, labeling, drug listings; the registration database; and the veterinary compendium; ...
Freelance Senior Regulatory Affairs Specialist
The Senior Regulatory Operations Specialist position is an integral part of MRM for Health and the Regulatory Operations capability. Regulatory Operations is accountable and responsible for the preparation, review, and submission of regulatory packages to Client Medical, Legal and Regulatory (MLR) g...
Regulatory Affairs Specialist
Minimum 5 years of experience in Regulatory Affairs, Quality Assurance or related field or any combination. ...
Investigative Director, Specialist Team - All FINRA Locations
The Director develops and supervises specialists regulatory programs and work products related to the routine and special examinations/investigations and other reviews related to finances, policies, procedures, practices, and products offered by FINRA member firms and their associated persons. Ident...
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the developm...
Senior Principal Regulatory Affairs Specialist
Position Objectives:Responsible for the overall product strategy, reporting, administrative documentation, due diligence, market expansion, labeling content, regulatory compliance, regulatory intelligence and change management for consumer products (Rx/OTC, OTC Monograph, Nutritional, and Cosmetics)...
Regulatory Affairs Specialist
The requirement is for 3 Regulatory Affairs Specialist. The candidates will work with client & Our client's teams to deliver best in-class solutions for regulatory submissions. Facilitate worldwide product registration activities by compiling appropriate dossiers, submissions and responses to regula...
Veterinary Product Regulatory Specialist -VPRS24-08921
Veterinary Product Regulatory Specialist. The Veterinary Product Regulatory Specialist is responsible for maintaining US pharmaceutical product registrations and providing support for labeling and chemistry, manufacturing, and controls (CMC) submissions to the Center for Veterinary Medicine (CVM) an...
Institutional Compliance Officer-Regulatory Specialist
Rutgers, The State University of New Jersey is seeking an Institutional Compliance Officer, Regulatory Specialist (RSCO) for University Ethics and Compliance. ...
Regulatory Affairs Specialist (Hybrid)
Regulatory Affairs Specialist (Hybrid) . Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey. Provide Regulatory Documentation Support to Global RA team members for Product Registrations, Renewals, etc. Experience in Regulatory Aff...
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
Job Title: USA-Regulatory Affairs Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology...
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the developm...
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Regulatory Affairs Project Lead, fully rem...
Staff Regulatory Affairs Specialist, International (Remote)
Represent international RA and demonstrate leadership in complex product development strategies by identifying and interpreting relevant regulatory requirements, and providing actionable regulatory guidance throughout the product development cycle prior to regulatory submission. Review protocols and...
Regulatory Affairs Specialist (Hybrid)
Regulatory Affairs Specialist (Hybrid). Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey. Provide Regulatory Documentation Support to Global RA team members for Product Registrations, Renewals, etc. Experience in Regulatory Affairs pr...
Regulatory Affairs Specialist II
This position is responsible for the preparation of regulatory submissions required to market medical devices in both the and Europe, support of international product registrations and related regulatory affairs activities, including execution of procedures and systems designed to ensure that the pr...
Specialist - Regulatory Compliance
The Regulatory Compliance Specialist will contribute to our organization success by ensuring the organization adheres to legal and relevant regulatory requirements by partnering cross-functionally with internal and external partners. Support the maintenance of regulatory files and internal tracking ...
Regulatory Affairs Specialist Project Lead
This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Early Development. Additionally, this role leads the developm...
Regulatory Affairs Specialist
Coordinate regulatory activities with internal teams and external regulatory agencies. Proven experience in leading regulatory submissions and managing regulatory projects. Oversee the day-to-day functions of the regulatory initiatives for Hassen Implants, Digital, and Biomaterial Solutions. Develop...
Sr. Specialist, Regulatory Affairs (Onsite)
Specialist, Regulatory Affairs. Specialist, Regulatory Affairs to join our team. The candidate will be responsible for providing expert support in applicable team meetings and when consulted, and operate as a SME regarding regulatory guidances/regulations and strategies to other members of the regul...
REMOTE Regulatory Affairs Specialist
The Regulatory Affairs Specialist will assist in providing regulatory services to management for the Global Regulatory Affairs (GRA) group throughout the functional operations of improving entire drug development and commercialization process in areas including document authorship and review, prepar...
Regulatory Affairs Biologicals labeling specialist
Prepare new/revised label packaging for regulatory submissions to the USDA and maintain regulatory documents to ensure site compliance. Support regulatory filing submissions with the USDA for both domestic and international product packaging. ...
Regulatory Affairs Specialist (Hybrid)
Regulatory Affairs Specialist (Hybrid) . Kelly® Science & Clinical is seeking a Regulatory Affairs Specialist for our client in Bridgewater, New Jersey. Provide Regulatory Documentation Support to Global RA team members for Product Registrations, Renewals, etc. Experience in Regulatory Aff...
USA-Regulatory Affairs Specialist Project Lead I (Scientific)
Regulatory Affairs Specialist Project Lead I (Scientific). This role will be accountable for leading the development and execution of innovative and value-added global regulatory strategies and be responsible for formulating the Global Regulatory Project Strategy (GRPS) for immunology products in Ea...
Sr Specialist, Regulatory Planning and Publishing, Digital Innovation and System
Overview:**The Regulatory Planning and Publishing (RPP) Organization within Global Regulatory and Clinical Safety- Operations Process and Systems (GRACS-OPS) is responsible for the execution of regulatory strategy to get and keep products on the market through the authorization, planning, and manage...