Manager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
read moreManager, Operational QA, responsible for Developing and implementing labeling processes and procedures and collaborating with cross-functional teams, including Clients, Regulatory Affairs, and Marketi...
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 moreIntegration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects and coordinate post- integration RA activities such...
read moreHandle regulatory submissions, CAPAs, customer complaints, conduct regulatory reviews, and participate in audits to verify compliance with procedures and regulations. Experience with regulatory submis...
read moreHandle regulatory submissions, CAPAs, customer complaints, conduct regulatory reviews, and participate in audits to verify compliance with procedures and regulations. Assist the Director of Quality Op...
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. Class II or III medi...
read moreRegulatory Affairs Project management experience. Integration liaison role between Global/Regional/Local RA and cross-functional team members to streamline, manage and track all integration projects a...
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 moreThe Senior Specialist Regulatory Affairs executes on the pharmaceutical regulatory strategies for assigned brand products. Liaise with country-specific regulatory affairs personnel for international s...
read moreAbout the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. Regulatory Affairs experience or related experience in a regulated environment.
Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and experience. Pesticide Regulatory Affairs Specialist re...
read moreAbout the job Regulatory Affairs Specialist I. Regulatory Affairs Specialist I. Regulatory Affairs experience or related experience in a regulated environment.
The Senior Specialist Regulatory Affairs executes on the pharmaceutical regulatory strategies for assigned brand products. Strong business acumen and ability to see the business drivers outside of Reg...
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 moreRegulatory Affairs Specialist duties:. About the job Pesticide Regulatory Affairs Specialist. Pesticide Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or ...
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 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 moreSupport internal and external Regulatory agency audits, providing Regulatory input to minimize potential findings of non-compliance. Stay abreast of Regulatory procedures and changes in the Regulatory...
read moreTechnology Regulatory Affairs Specialist.
Technology Regulatory Affairs Specialist.
Change Management Regulatory Impact Assessment: Provide regulatory assessments for post approval change proposals, filing strategies and timelines. Maintain regulatory information in accordance with p...
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 moreFamiliarity with regulatory affairs and submission management tools, regulatory submission tracking, and compliance management. Proficiency in preparing regulatory submissions such as 510(k) (U. Globa...
read moreThe Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of ...
read moreThe Regulatory Affairs Specialist (F&B) will be responsible to independently provide Symrise Inc. The Regulatory Affairs Specialist may provide support to the retrieval of revenue paid for the use of ...
read morePerforms quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) ...
read morePerforms quality control, research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring that Good Clinical Practices (GCP) ...
read moreEligibilities & qualifications.
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 dom...
read moreConduct routine Regulatory audits of Henry Schein facilities, affiliates and subsidiaries. Regulatory knowledge of controlled substances, list 1 chemicals and other regulated products is a strong plus...
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