Medical Device Regulatory Affairs Jobs in Deerfield, IL

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

from: Lundbeck (+1 source) - More than 30 days ago

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

from: Lundbeck (+1 source) - More than 30 days ago

Baxter International Inc - Deerfield, Illinois, USA

projects, transactions, or matters. Serves relevant business leadership and other law department members as a key advisor in defined areas of medical device and pharmaceutical regulatory law. In addition $216,000 to $324,000

from: Ivyexec.com - 22 days ago

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

from: Lundbeck - More than 30 days ago

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

from: linkedin.com - 23 days ago

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

from: linkedin.com - 25 days ago

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

from: resume-library.com - 17 days ago

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

from: linkedin.com - 20 days ago

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

from: resume-library.com - 21 days ago

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

from: resume-library.com - 2 days ago