Latest Product Management Medical Device jobs in Cincinnati, OH

6 Product Management Medical Device Jobs in Cincinnati, OH

Director Quality Assurance and Regulatory Affairs Gateway Recruiting - Gateway to Global Careers - Contingent, Retained, Contract Recruiting Services - Cincinnati, OH, United States of the Regulatory Affairs Processes, Registration, Non-Conformities, Product Recalls, and Medical Device Reporting (EUMDR). Act as Person Responsible for Regulatory Compliance (PRRC). Maintain an effective quality 29 days ago
Clinical Research Associate - Clinical Research Coordinator Experience Medpace, Inc. - Cincinnati, Ohio that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious 25 days ago
Marketing Manager, Global Strategic Marketing Johnson and Johnson - Cincinnati, OH relationships is required. * Demonstrated teamwork and influence management are required. * Previous medical device marketing, Global Strategic Marketing, and/or healthcare sales experience is highly preferred 9 days ago
Clinical Research Associate (CRA) - Cincinnati, OH Medpace, Inc. - Cincinnati, OH that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious 25 days ago
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Marketing Manager, Global Strategic Marketing Johnson & Johnson - Cincinnati, OH teamwork and influence management are required. Previous medical device marketing, Global Strategic Marketing, and/or healthcare sales experience is highly preferred. Experience in brand management USD 99,000.00 - 170,200.00 per year 20 days ago
Clinical Research Associate - Clinical Research Coordinator Experience Cincinnati, OH that the investigator is enrolling only eligible subjects; Regulatory document review; Medical device and/or investigational product/drug accountability and inventory; Verification and review of adverse events, serious More than 30 days ago

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