Latest Medical Device Regulatory Affairs jobs in Deerfield, IL

16 Medical Device Regulatory Affairs Jobs in Deerfield, IL

Associate Director of Neurology HCP Marketing - Remote Opportunity Lundbeck - Deerfield, Illi, US Ensure all marketing projects are compliant and have obtained necessary approvals through the appropriate medical, legal, and regulatory review processes Achieve alignment through collaboration More than 30 days ago
Director US Regulatory Global Strategic Labelling - Remote Opportunity Lundbeck - Deerfield, Illi, US ). REQUIRED EDUCATION, EXPERIENCE AND SKILLS: Accredited Bachelor’s Degree 10+ years of experience within a pharm aceutical, medical device and/o r biotech industry, with 7+ years of experience in Regulatory More than 30 days ago
Associate Director VYEPTI Consumer Marketing Lundbeck - Deerfield, IL through collaboration and communication with: brand leadership, data & analytics, market research, sales training, finance, regulatory affairs, product communications, and other cross-functional partners 18 days ago
Regulatory Affairs Specialist GForce Life Sciences - Lake Forest, IL, United States combination of education and experience. 4+ years’ experience in Regulatory Affairs role. Strong knowledge of IVDR and EU regulatory requirements is required. 1+ years’ experience in an IVD or medical device 23 days ago
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Regulatory Affairs Manager Catalyst Life Sciences - Chicago, IL, United States materials for accuracy, comprehensiveness, and compliance with regulatory standards. Experience Required 6 years' Regulatory Affairs experience within Medical Devices or IVDs, understanding FDA requirements 25 days ago
Regulatory Specialist II Experis - Lake Forest, Illinois to the Regulatory Affairs organization by – Responsible for technical writing of files by In Vitro Diagnostic Medical device Regulation (IVDR). Provides regulatory support for diagnostic product development 7 days ago
Director, Safety. Regulatory Affairs and Medical Affairs Quality Standards AbbVie - North Chicago, Illinois is responsible for the management of a RDQA global Safety, Regulatory Affairs (RA) and Medical Affairs (MA) QA team which provides independent quality oversight of GxP activities, covering the AbbVie drug, device 5 days ago
Senior Manager, Medical Affairs Quality ( On-site, IL based) North Chicago, IL in the pharmaceutical, medical device/nutritional or related industry. Four years in compliance/auditing or regulatory affairs is desirable. Total combined experience expected to be at least 10 years. ASQ certification 10 days ago
Hybrid Senior Manager, Regulatory Affairs Clagam Global Solutions LLC - Lincolnshire, Illinois . Responsibilities: We currently have a great opportunity available for a Regulatory Affairs Senior Manager. This role involves leading the regulatory strategy for new and modified medical device products. The Senior 22 days ago
Senior Manager, Medical Affairs Quality ( On-site, IL based) AbbVie - North Chicago, Illinois , including but not limited to non-interventional studies, medical information and other regulatory commitments., covering the AbbVie drug, device and cosmetic portfolio. The role reports to a Director 11 days ago

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