;Development process generic->Medical Device development process->ISO 13485,Technology->Quality models/improvement...Responsibilities : "• Be a part of core project team and support the quality engineering across the entire...
and coordinate trials in internal and external labs. Assist project teams in establishing specifications and quality standards... Preferred Skills : Foundational->Quality Assurance->Quality Assurance Educational Requirements : Bachelor...
: Understanding of Medical Device Regulatory Compliance (ISO 13485, CFR 820, or comparable standard / regulation) and EU's Medical... the Quality function across teams Preferred ASQ Certified Quality Engineer (CQE). Commodity Domain Knowledge...
product development process. Work Experience Requirements 8+ years of design assurance medical device experience... is required. Relevant experience in the medical device industry Education Requirements Degree in Engineering/Science Discipline...
: Required: Experience on Quality Management (ISO 13485 or 21 CFR 820) Understanding on Medical Device Risk Management; New Product... in Medical Device/Automotive/Manufacturing domain. Travel Percentage: 10%...
regulations; Medical Device Risk Management Hands-on Experience on Complaint handling and Product investigations of medical... in Bio Medical / Mechanical Engineering / Electrical Engineering or related field from premier institutes experience- 2years...
JobType: full-time We are seeking an experienced C++ Engineer with a strong background in medical device software..., medical imaging, and safety-critical systems to deliver high-quality, scalable applications. Requirements...
and an ISO 13485 environment at a medical device manufacturer (preferred) · Project management training and experience...work mode: hybrid work location: sector 43, gurgaon SUMMARY The Sr.Core Business Support Engineer II will lead...
or Biomedical 4-7 years of work experience Medical device background in Design and development Endovascular/Vascular desi..., develop, modify, and verify components/modules for medical devices Translate design inputs to engineering specifications...
medical device regulations (e.g. CDSCO, ISO 13485/Indian GMP, US FDA, EU MDR). The QA/RA Director will oversee product..., preferably in the healthcare industry and ideally within the MedTech sector. Strong understanding of the Indian Medical Device...