Search current Full-time fda jobs, vacancies, and employment in Pune, India on Jobeax. Full-time fda jobs in Pune, India.
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BPL Medical Technologies
... balancing electrical, mechanical, and biocompatibility requirements while ensuring designs meet stringent safety and regulatory standards (IEC 60601, ISO 13485, FDA 510(k)/PMA pathways). Lead System Design & Engineering Lead the end-to-end design of external defibrillator electrode/lead systems, including pad electrodes, ...
India, Bengaluru
... able to envisage new and better ways of doing things. - Excellent analytical skills, ability to plan, organise and implement concurrent tasks. - Experience in an FDA regulated or regulated industry beneficial. - High level of PC Skills required. - Fundamental knowledge and understanding of mechanical engineering practices ...
India, Noida
samasta foods
22137 - 50k
... custom formulations. - A 50,000 sq ft fully automated plant in Jaipur, scaled from a 5,000 sq ft manual operation in five years. - BRCGS Grade A, FSSC 22000, US FDA, EU Organic, USDA Organic/NOP, NPOP, Kosher, GMP, Halal and SEDEX/SMETA — more than ten active certifications. - A farmer network of 500+ certified farmers and ...
India, Jaipur
... You'll define and advance quality and compliance strategies for SAP products and cloud services, ensuring alignment with global regulatory frameworks such as FDA 21 CFR Part 11, EU Annex 11, ICH guidelines, and GAMP 5. Your expertise will help SAP and its customers confidently adopt innovative technologies while maintaining ...
India, Bengaluru
... requirements are incorporated into product design, development, verification, validation, and post-market activities. Support regulatory activities associated with FDA, EU MDR, UK MDR, UKCA, MHRA, Health Canada, MDSAP, and other applicable global regulatory frameworks. Author and maintain regulatory documentation including technical ...
India, Bengaluru
... subtractive machining, anodization, additive manufacturing, forging, casting, plastic molding) and material science for application in new product development desired - FDA QSR and EU MDR medical device regulatory requirements, and industry/regulatory body recognized technical product standards knowledge desired - Statistics knowledge ...
India, Bengaluru
... requirements are incorporated into product design, development, verification, validation, and post-market activities. - Support regulatory activities associated with FDA, EU MDR, UK MDR, UKCA, MHRA, Health Canada, MDSAP, and other applicable global regulatory frameworks. - Author and maintain regulatory documentation including ...
India, Bengaluru
... subtractive machining, anodization, additive manufacturing, forging, casting, plastic molding) and material science for application in new product development desired FDA QSR and EU MDR medical device regulatory requirements, and industry/regulatory body recognized technical product standards knowledge desired Statistics knowledge ...
India, Bengaluru
Job Title: Regulatory & Technical Writer Experience 1–2 years (hands-on ownership in Regulatory [CDSCO, ISO, FDA] documentation) About the Role We are seeking an experienced Technical Writer to support our AI team with regulatory and compliance documentation for AI-enabled medical devices and software (SaMD). This role ...
India
25k
... treatment of AVN, chronic back, neck, and knee pain, the center has successfully helped over 25,000 patients avoid surgery with a 90% success rate. Using advanced FDA-approved technologies, such as high-power lasers, targeted robotics spinal disc decompression, and regenerative medicine, the center focuses on repairing and ...
India, Delhi