192 Medical Device Regulatory Affairs Jobs - page 2
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Regulatory Affairs Manager SS White Dental - Lakewood, NJ, United States disciplines Requires minimum 5 years of regulatory experience in a medical device manufacturing environment with a proven track record of obtaining regulatory agency approvals. Regulatory Affairs Certification 3 days ago
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Regulatory Affairs Specialist (APAC) ACE Partners - , PA, United States requests Basic Qualifications: 2+ years Medical Devices Regulatory Affairs Experience History of successful international APAC device registration (China, Korea, Japan) Experience in preparing US 510(k 18 days ago
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Laboratory Technician Collabera - Minneapolis, MN, United States procedures and regulatory requirements. Complete FDA Medical Device Reporting (MDR) submissions and other regulatory reports for competent authorities. Collaborate cross-functionally with other departments 3 days ago
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Director Clinical Affairs Walker Cole International - , MA, United States Required experience for the Director of Clinical Affairs: years of clinical research experience years of medical device clinical research experience in the USA, including IDE and post-market understanding 9 days ago
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Lead Mechanical Engineer - Lyophilizers i-Pharm Consulting - Indianapolis, IN, United States has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Quality Assurance and Bioinformatics. www.i-pharmconsulting.com TO APPLY If you would like to discuss 5 days ago
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Regulatory Affairs Manager EPM Scientific - San Jose, CA, United States Title: Regulatory Affairs Manager Location: San Jose, CA Base Salary: $140,000-$190,000 About: Currently working with a medical device company dedicated to developing and commercializing breakthrough 23 days ago
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Regulatory Affairs Specialist Highridge Medical - Westminster, CO, United States device industry preferred. A minimum of 3 years of experience in Regulatory Affairs, Engineering, Quality, or related field required. Regulatory Affairs Certification (US or EU) preferred. A combination 11 days ago
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Quality Systems Analyst- St. Paul, MN MGC Diagnostics - St Paul, MN, United States , Scientific, or Engineering discipline 5-7 years of experience in Quality Assurance, Regulatory Affairs, or other Quality Systems role, preferably in medical device or other regulated industry. Knowledge of ISO 5 days ago
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Regulatory Affairs Specialist GForce Life Sciences - Santa Clara, CA, United States Regulatory Affairs Specialist II – Santa Clara, CA Must be able to work on a W2 Job Summary We're looking for a Regulatory Specialist with 2-5 years of experience in the medical device industry 9 days ago
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Director of Clinical Services ACE Partners - , MN, United States Our client are looking for a Director of Clinical who has hands-on industry experience in both Clinical Affairs & Clinical Services for their high-risk Medical Device & IVD CRO. Duties Direct 5 days ago
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