Latest Medical Device Regulatory Affairs jobs in Lincolnshire, IL

16 Medical Device Regulatory Affairs Jobs in Lincolnshire, IL

Sr. Specialist - Cybersecurity, Regulatory Affairs Sysmex - Lincolnshire, Illinois software and cybersecurity framework and procedures to maintain and ensure compliance with medical device regulatory requirements. The individual will coordinate and collect specific product registration 17 days ago
Manager, Regulatory Affairs Sysmex - Lincolnshire, Illinois Affairs contributes to the regulatory strategy for new and modified Sysmex medical device products. The individual will need to identify, assess and communicate regulatory development, submission strategies 21 days ago
Hybrid Senior Manager, Regulatory Affairs Clagam Global Solutions LLC - Lincolnshire, IL, United States . 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 More than 30 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
Director, Safety, Vigilance and Medical Affairs, Quality Assurance Lead AbbVie - North Chicago, Illinois safety, maintains data integrity, fosters regulatory compliance, and contributes to the overall success of drug/device development programs. Director, Medical Affairs Quality Assurance is responsible 2 days ago
Senior Consultant, Pharma/ Medical Device (Regulatory and M&A Consulting Solutions) Kamet Consulting Group - Chicago, IL, United States of five years of work experience related to the Regulatory Affairs, Regulatory Operations, Supply Chain, or Labeling Operations within the pharmaceutical and/or medical device industry Prior consulting 20 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, Illi, US collaboration and communication with: brand leadership, data & analytics, market research, sales training, finance, regulatory affairs, product communications, and other cross-functional partners REQUIRED More than 30 days ago
Section Head - Medical Writing Abbott Laboratories - Chicago, Illinois and international medical device regulatory submissions. Challenges conclusions when necessary. Effectively develops and communicates timelines to manager and collaborates with R&D, Regulatory Affairs, Quality Yesterday

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