Iso13485 Jobs

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SENIOR QA/RA EXECUTIVE  

GPC Medical Ltd. - Delhi, India

all over the globe. The company is ISO 13485 Certified, WHO-GMP Compliant, and many of its products are CE Marked. GPC Medical specializes in Orthopedic Implants, Medical Disposables, Hospital Furniture

from: linkedin.com - 2 days ago

Mechanical Engineer (Medical Devices)  

Molex - Bengaluru, Karnataka, India

, following the Phillips-Medisize Design Development Process (DDP) and applicable standards such as ISO 13485 with design controls, ISO 14971 and appropriate ASME standards. Essential Functions Operate primary

from: linkedin.com (+1 source) - 14 days ago

QC Specialist  

Shree Umiya Surgical - GIDC Estate Vatva, Ahmedabad Region

Develop and maintain a Quality Management System in accordance with domestic and international medical device regulatory requirements (FDA, ISO13485, MDD etc.) Perform physical & Chemical tests ₹14,000 - ₹21,000 monthly

from: apna.co - 3 days ago

Senior Quality Assurance  

Indegene - Bengaluru, Karnataka, India

and Responsibilities: Develop, implement, and maintain quality system documentation (SOPs, WIs, templates, forms) adhering to QMS requirements and regulations (ISO 13485, 21 CFR 820). Conduct a thorough gap analysis

from: linkedin.com (+1 source) - 16 days ago

Medical Device Engineer / Senior Medical Device Engineer  

Anumana - Bengaluru, Karnataka, India

, Traceability Matrices and Final Reports. Support development projects meet defined development process requirements of FDA 21 CFR 820.30, EN/ISO 13485:2016 and IEC 62366-1. Support software development

from: linkedin.com (+1 source) - 17 days ago

Sr. Executive - RA  

Quality HR Services - Daman - Diu

Position: Sr. Executive - RALocation: DamanExperience: 8 to 12 YearsIndustries: Pharma Responsibilities:Maintaining compliance with ISO 13485, MDD, and MDR requirements.Preparing technical and device 7.00 LPA To 8.00 LPA INR

from: jobitus.com - 7 days ago

Quality Analyst Lead  

Indegene - Bengaluru, Karnataka, India

practices. Strong working knowledge of design documentation for all types of medical devices, including standalone software. Deep understanding of ISO 13485:2016, 21 CFR 820, and risk management principles

from: linkedin.com (+1 source) - 16 days ago

Head of Clinical Research  

Dozee - Bengaluru, Karnataka, India

and home to drive automation of vitals collection and AI driven early warning system to drive patient triaging Certifications & Accreditations : ISO13485:2016 Certified, ISO27001:2013 Certified, CDSCO

from: linkedin.com (+1 source) - 16 days ago

Associate Director Regulatory Affairs MoS  

Pimpri-Chinchwad, Maharashtra, India

, MedDev’s, FDA QSR’s, ISO 13485 & 14155, and other applicable major/regional worldwide regulations. Working knowledge in regulations concerning device labeling as well as advertising and promotion Shown

from: jobleads.co.in - Yesterday

Design And Development Engineerer  

Meril - Vapi, Gujarat, India

Regulations like ISO 13485, ISO 14971 7.Assist in the creation of verification and validation plans, protocols, and reports. Oversee testing and analysis for standards and product requirements compliance

from: linkedin.com - 26 days ago


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