Minnesota > St. Paul > Lillehei : One Lillehei Plaza ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Continuous...
We anticipate the application window for this opening will close on - 19 May 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare...
We anticipate the application window for this opening will close on - 19 May 2025 At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare...
Supports all business segment initiatives as identified by divisional management and in support of QualityManagementSystems (QMS), Environmental Management Systems (EMS), and other regulatory requirements...
Starting Salary Range: $80,000-96,000 - position is also eligible for an annual bonus if individual performance and company objectives are met. In one year as our Compliance Analyst, you will know...
Management District (SCAQMD), and Ozone Transport Commission (OTC) Volatile Organic Compound (VOC) rules/regulations and requirements Experience with systems/business processes relevant to Regulatory...
Systems standards and clinical investigations Solid understanding and knowledge of product development process, clinical development, manufacturing, and change control Demonstrated experience authoring...
Minnesota > St. Paul > Lillehei : One Lillehei Plaza ADDITIONAL LOCATIONS: WORK SHIFT: Standard TRAVEL: No MEDICAL SURVEILLANCE: No SIGNIFICANT WORK ACTIVITIES: Continuous sitting for prolonged...
. + Own audit readiness and guide teams through federal and state exams, internalaudits, and testing processes with confidence and clarity. + Turn insights into action by analyzing results, delivering...
Job Description: Job Title Trade Compliance Analyst Free Trade Agreements Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your...
Food and Drug Administration (FDA) regulations, international regulations and other regulatory requirements, company policies, operating procedures, processes, and task assignments....
Submit product and qualitysystem changes to the notified body. Participate in regulatory training and transfer the information back to the Regulatory department providing insightful application....
Experience of working within the requirements of 21CFR820, ISO 13485, the Medical Devices Directive (93/42/EEC) and/or the IVD Directive (98/79/EC)....
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Regulatory Affairs Specialist Online Courses and Training Opportunities
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OverviewDrug Regulatory Affairs (DRA) is a field that involves the study and implementation of regulations, guidelines, and laws related to the development, production, and marketing of...
This course provides an overview of the Chemistry, Manufacturing and Controls (CMC) section of dossiers and discusses CMC information necessary to support product applications, identifies CMC...
OverviewA Medical Devices and Regulatory Affairs course is a program of study that covers the regulation and compliance requirements for medical devices in various countries, including the United...
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