Job Title: Regulatory Affairs Specialist. Regulatory Formula Creation utilizing Excel to create a regulatory formula for use in global dossier documents. Provide support in regulatory related product ...
read moreRegulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program, which consistently delivers high qu...
read moreRegulatory Affairs Specialist* This position assists the Director of Quality Operations (DQO) in maintaining an effective Quality Operations and Regulatory Program, which consistently delivers high qu...
read moreAbout the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. Global - Responsible for the overall product strategy, global reporting, administrative documentation, due diligence, ma...
read moreProvide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Provi...
read moreProvide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Provi...
read moreThe Regulatory Affairs Specialist will review and approve Dietary Supplement/Food labels for technical accuracy and compliance to all mandated regulatory requirements, provide information to rectify l...
read moreRegulatory Formula Creation utilizing Excel to create a regulatory formula for use in global dossier documents. Veeva Technical Input utilizing Veeva software to create those regulatory sections of pa...
read moreThe Regulatory Affairs Specialist will provide leadership and strategic direction for global regulatory compliance activities. The Regulatory Affairs Specialist will work closely with cross-functional...
read moreSupport regulatory impact assessments for change controls and other Regulatory Affairs/Quality Assurance items from a review and approval level. As a Staff Regulatory Affairs Specialist in Advertising...
read moreThe Regulatory Affairs Specialist will provide leadership and strategic direction for global regulatory compliance activities. The Regulatory Affairs Specialist will work closely with cross-functional...
read moreRegulatory Formula Creation utilizing Excel to create a regulatory formula for use in global dossier documents. Veeva Technical Input utilizing Veeva software to create those regulatory sections of pa...
read moreAbout the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. Global - Responsible for the overall product strategy, global reporting, administrative documentation, due diligence, ma...
read moreJob Title: Regulatory Affairs Specialist. Provide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulatio...
read moreProvide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Veeva...
read moreProvide support in regulatory related product life-cycle review activities, preparation of regulatory documentation and ensuring compliance with all regulations of Hill's Pet Nutrition products. Veeva...
read moreSenior Regulatory Affairs SpecialistThe Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Responsibilities* Prov...
read moreSenior Regulatory Affairs SpecialistThe Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Responsibilities* Prov...
read moreAs a Regulatory Affairs Specialist, you will play a pivotal role in monitoring regulatory developments, ensuring compliance, and driving regulatory excellence across multiple product categories, inclu...
read moreAs a Regulatory Affairs Specialist, you will play a pivotal role in monitoring regulatory developments, ensuring compliance, and driving regulatory excellence across multiple product categories, inclu...
read morePrincipal Regulatory Affairs Specialist,. Principal Regulatory Affairs Specialist,. This position requires extensive expertise in regulatory frameworks, strategic planning, and cross-functional collab...
read moreQuality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...
read moreThe Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achieving domestic and regulatory approval. Experience: 15+ years of experience in regulatory affa...
read moreThe Senior Regulatory Specialist must be experienced and thoughtful about the processes necessary for achieving domestic and regulatory approval. Certifications: RAC (Regulatory Affairs Certification)...
read moreThe Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Senior Regulatory Affairs Specialist. Class II or III medi...
read moreThe Senior Regulatory Affairs Specialist is responsible for planning and executing regulatory submissions and ensuring regulatory compliance. Senior Regulatory Affairs Specialist. The individual combi...
read moreAbout the job Pesticide Regulatory Affairs Specialist. Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and...
read moreAbout the job Pesticide Regulatory Affairs Specialist. Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and...
read moreStay abreast of Regulatory procedures and changes in the Regulatory climate. Support internal and external Regulatory agency audits, providing Regulatory input to minimize potential findings of non-co...
read moreMaintain regulatory information in accordance with processes and procedures to support regulatory compliance. Change Management Regulatory Impact Assessment: Provide regulatory assessments for post ap...
read moreChange Management Regulatory Impact Assessment: Provide regulatory assessments for post approval change proposals, filing strategies and timelines. Maintain regulatory information in accordance with p...
read moreQuality and Regulatory Affairs Specialist. Participates in the preparation, planning, coordination and oversight of planned and unplanned regulatory survey and reporting by The Joint Commission, New Y...
read moreQuality and Regulatory Affairs Specialist. The Quality and Regulatory Specialist facilitates and participates in the implementation of the multidisciplinary hospital and system wide Clinical Quality a...
read moreThe Regulatory Affairs Specialist will support the Director of Regulatory Affairs and collaborate with various departments to complete international product registrations (Canada, Southeast Asia, Midd...
read moreSupport daily Regulatory Affairs function eg; compliance to CFR ,, ISO requirements, Company policies, operating procedures, processes, promotional task assignments into windchill and assigned trainin...
read moreCertification is a plus (such as RAC from the Regulatory Affairs Professionals Society. Anticipate regulatory obstacles and emerging issues throughout the product submission. Provide regulatory input ...
read moreThe Specialist Regulatory Affairs is responsible for ensuring that the assigned Brand products meet and follow all regulatory requirements necessary to conduct business globally. Ensuring outgoing Reg...
read moreRegulatory 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 res...
read moreRegulatory Affairs Specialist Project Lead I (Scientific). At least - years of relevant pharmaceutical/biotechnology experience in R&D, including at least years of relevant Regulatory Affairs experien...
read moreAt least 8-10 years of relevant pharmaceutical/biotechnology experience in R&D, including at least 5 years of relevant Regulatory Affairs experience (regionally and/or global), in early development. T...
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