Latest Medical Device Regulatory Affairs jobs in Lake Forest, IL

13 Medical Device Regulatory Affairs Jobs in Lake Forest, IL

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
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
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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
Regulatory Affairs Specialist II - 5 Openings DivIHN Integration Inc - Lake Forest, IL in Regulatory Affairs role. Strong knowledge of IVDR and EU regulatory requirements is required. PREFERRED QUALIFICATIONS: 1 years' experience in an IVD or medical device manufacturing environment. COMPETENCIES 20 days ago
Regulatory Affairs Associate DivIHN Integration Inc - Lake Forest, IL . Experience: 4 years' experience in Regulatory Affairs role; Strong knowledge of IVDR and EU regulatory requirements is required. Preferred Experience: 1 years' experience in an IVD or medical device $29.50 - $31.00/Hour 21 days ago
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, Medical Device & Combination Product NPI Quality AbbVie - North Chicago, Illinois Job Description Purpose Responsible for quality oversight for late-stage development and new product introduction of combination products and medical devices. Scope of responsibility can also include 5 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

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