| Job alert | Jobs 51 - 57 of 57 |
System Engineer-Medical Devices
Excellence and Eminence LLP
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Bengaluru, Karnataka, India
Upto 18 LPA
... Key Skills Systems engineering, medical device development, system integration, risk management, ISO 13485 and FDA 21 CFR Part 820. Responsibilities - Lead systems engineering efforts for medical device development from concept to commercialization. ... - Sep 20
Sr Staff Technical Program Manager
Gehc
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Sadduguntepalya, Karnataka, 560029, India
... Familiarity with ISO, FDA and other regulatory standards. Strong knowledge of SDLC, software design and implementation skills Setting the strategy and direction of the business and driving continuous improvement of systems, products and processes. ... - Sep 05
Cybersecurity-Strategy Risk & Compliance-Manager-Bangalore
Pwc
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Bengaluru, Karnataka, India
... This includes, but is not limited to: NIST CSF, ITIL, HIPAA, PCI, FDA, FERC/NERC, OCC, FFIEC, ABAC, Cyber Executive Orders, etc. Our team designs, implements, and maintains an effective compliance program that helps our clients manage the risks ... - Sep 17
Regulatory Affairs Associate
Dozee
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Bengaluru, Karnataka, India
... Ensure compliance with FDA, ISO 13485, MDR, and other relevant regulatory requirements. Maintain awareness and understanding of new and existing regulatory requirements. Support identification of applicable regulatory requirements, their impact and ... - Sep 23
PSR - Product Security Representative (Code OOEE)
SSS Grameen Services
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Bengaluru, Karnataka, India
... · The released products shall be in compliance to required regulatory standards & compliance (like FDA, HIPPA, GDPR etc) · Works with the Product Security team and QARA-Quality Assurance & Regulatory Assurance on released product life cycle, ... - Aug 30
Software Engineer, Managed Services
SingleStore
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Bengaluru, Karnataka, India
... Please note that SingleStore’s COVID-19 vaccination policy requires that team members in the United States be up to date with the current CDC guidelines for their vaccinations with one of the United States FDA-approved vaccine options to meet in ... - Sep 05
Medical Reviewer
MMS Holdings Inc.
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Indiranagar, Karnataka, 560008, India
... Demonstrate strong knowledge of current clinical trial and post market PV regulations (ICH, GVP, EMA, FDA, etc) Provide significant expertise as primary medical reviewer of individual case safety reports (ICSRs), including reportability and ... - Aug 24