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)....
Minnesota > Plymouth : 5050 Nathan Lane N ADDITIONAL LOCATIONS: United States > Minnesota > St. Paul > Tech Center : One St Jude Medical Drive WORK SHIFT: Standard TRAVEL: Yes, 5 % of the Time...
Systems standards Prior experience with a variety of regulatory submissions for US and EU MDR Previous experience interacting with regulators and leading initiatives across functions, divisions, or...
Join our dynamic team as a Trade Compliance Analyst, where you'll play a crucial role in ensuring seamless operations and compliance with international trade regulations. This position offers a...
HealthPartners is currently hiring for a Benefits Compliance Analyst. The analyst ensures that HealthPartners remains compliant with the Affordable Care Act (ACA) and other regulatory requirements...
The Principal RegulatoryAffairsSpecialist develops strategies for worldwide product registration with global regulatory agencies to introduce Diagnostics products and External Pacemaker to market,...
Supports all business segment initiatives as identified by divisional management and in support of QualityManagementSystems (QMS), Environmental Management Systems (EMS), and other regulatory requirements...
Number of Job Openings Available: 1 Date Posted: May 14, 2025 Department: 16007900 Allina Pharmacy Services Shift: Day (United States of America) Shift Length: 8 hour shift Hours Per Week: 40...
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...
Are you someone who loves to be an integral part of everyday business? If so, look no further and apply below for an opportunity to join a global organization that delivers care! Adecco is...
Job Description: Senior Regulatory Affairs Associate Collaborate with Innovative 3Mers Around the World Choosing where to start and grow your career has a major impact on your professional and...
Systems standards and clinical investigations Solid understanding and knowledge of product development process, clinical development, manufacturing, and change control Demonstrated experience authoring...
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Regulatory Affairs Specialist Online Courses and Training Opportunities
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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...
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...
Section 1-Regulatory affairs profesion -organization of different departments in pharmaceutical industry -Introduction to Common Technical Document (CTD)-Background on ICH guidance and CTD-Basic...
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