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...
Minimum 5 years of experience in Regulatory Affairs, Quality Assurance or related field or any combination. ...
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...
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...
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...
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 (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...
Catalent Pharma Solutions in Somerset, NJ is hiring a Senior Regulatory and Compliance Specialist for the Compliance Group. The Senior Regulatory and Compliance Specialist candidate must be knowledgeable in global regulations pertaining to the pharmaceutical industry and their impact on manufacturin...
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...
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...
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...
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...
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...
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...
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...
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...
Summary:**A Promotional Review Editor (PRE) of the Specialist level in US Commercial Regulatory Affairs Operations (CRA Ops) supports the Promotional Review Process (PReP) through a broad range of responsibilities and tasks, primarily by working directly with the US Commercial Brand teams. Regulator...
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...
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...
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...
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...
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 ...
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...
Regulatory Experience, 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. 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 ...
Rutgers, The State University of New Jersey is seeking an Institutional Compliance Officer, Regulatory Specialist (RSCO) for University Ethics and Compliance. ...