- Capgemini (Burlington, MA)
- …with relevant medical device regulations such as ISO 13485, IEC 62304, and FDA guidelines. . Defect Management: Lead root cause analysis and resolution of defects, ... privacy in medical systems. . Familiarity with medical device standards and regulatory requirements. . Proficiency in scripting and test automation tools (eg,… more
- Cole-Parmer (Franklin, MA)
- …product line development in collaboration with Research & Development, Operations, Regulatory Affairs and Commercial teams. Implement appropriate programs to either ... diagnostics, especially molecular diagnostics, applications + Industry-related experience in healthcare or laboratory-based life science markets preferably in diagnostics… more
- Rhythm Pharmaceuticals (Boston, MA)
- …for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage ... document control perspective in Veeva QDocs, ensuring documents meet procedural and regulatory requirements. + Participate in validation efforts for new or updated… more
- Rhythm Pharmaceuticals (Boston, MA)
- …for previously untreatable or undertreated diseases and provide meaningful support for healthcare providers and patients and their families. We recognize the courage ... 1-2 years of Drug Safety and Pharmacovigilance experience. + Knowledge of FDA , ICH, EU Regulations and Requirements for Pharmacovigilance required. + Solid… more