Quality & Regulatory Lead- Medical Devices
6 hours ago
Opportunity to lead QA RA for medical implants greenfield project Set up and maintain the Quality Management System in ISO 13485 About Our Client Global medical devices client in the space of orthopedic implants Job Description Regulatory Affairs: Lead interactions with Indian health authorities (CDSCO) for the registration and continued compliance of our implants and instruments. Oversee the regulatory process for the new facility certification. Quality System & Compliance: Set up and maintain the Quality Management System in alignment with ISO 13485 and corporate standards. Ensure compliance with national and international medical device regulations. Process & Equipment Qualification: Coordinate the qualification of industrial processes and validation of new equipment for production. Clinical Affairs: Manage and coordinate clinical investigations for products, in collaboration with corporate teams. Team Development: Recruit, train, and manage a growing quality and regulatory team to support operations and scale with business needs. The Successful Applicant Experience: 8+ years in quality and/or regulatory roles within the medical device industry, ideally with Class II or III implants. Prior experience in greenfield or startup manufacturing environments is a strong plus. Skills & Attributes: Deep understanding of ISO 13485, CDSCO regulatory frameworks, and international medical device compliance. Hands-on leadership style with a willingness to build and scale operations from scratch. Strong communicator with cross-cultural collaboration skills. Passionate about quality and patient safety, with a mindset for continuous improvement.
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Quality & Regulatory Lead- Medical Devices
5 days ago
Bangalore Division, India Michael Page Full timeOpportunity to lead QA RA for medical implants greenfield projectSet up and maintain the Quality Management System in ISO 13485About Our ClientGlobal medical devices client in the space of orthopedic implantsJob DescriptionRegulatory Affairs:Lead interactions with Indian health authorities (CDSCO) for the registration and continued compliance of our implants...
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Bangalore Division, India Michael Page Full timeDrive regulatory strategy with global impact at a leading healthtech innovatorLeadership role with strong visibility and growth potentialAbout Our ClientThis opportunity is with a global MNC recognized for its contributions to the life sciences industry.Job DescriptionRegulatory Strategy Development- Define and drive the regulatory vision and strategy for...
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Bangalore Division, India Michael Page Full timeDrive regulatory strategy with global impact at a leading healthtech innovator Leadership role with strong visibility and growth potential About Our Client This opportunity is with a global MNC recognized for its contributions to the life sciences industry. Job Description Regulatory Strategy Development- Define and drive the regulatory vision and strategy...
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Regulatory Affairs Specialist
11 hours ago
bangalore, India NexorTest Technologies Full timeLocation: Bengaluru / Hybrid Experience: 5 - 8 yearsOverall Package: 8 - 10 LPARole Summary:The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. The role involves working cross-functionally...
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bangalore, India Tek Support Full timeJob Title: Senior Trainer – Regulatory Affairs (Medical Devices)Location: RemoteJob Type: Part-TimeJob Summary:We are seeking an experienced Regulatory Affairs Trainer with deep expertise in medical device regulations and compliance to design and deliver advanced training programs for professionals in the medical device industry. The ideal candidate will...
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Regulatory Affairs Specialist
16 hours ago
bangalore, India NexorTest Technologies Full timeLocation: Bengaluru / Hybrid Experience: 5 - 8 years Overall Package: 8 - 10 LPA Role Summary: The Regulatory Affairs senior specialist will be responsible for planning, preparing, and managing regulatory submissions and compliance activities for medical devices under CDSCO (India), EU MDR, and US FDA frameworks. The role involves working...
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System engineer
2 weeks ago
Pune Division, India Tata Elxsi Full timeTata Elxsi is among the world’s leading providers of design and technology services across industries, including Automotive, Broadcast, Communications, and Healthcare. Tata Elxsi is helping customers reimagine their products and services through design thinking and the application of digital technologies such as IoT (Internet of Things), Cloud, Mobility,...
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Regulatory Affairs Specialist
1 week ago
bangalore, India Concept Medical Full timeAbout Us:Concept Medical is at the forefront of developing and manufacturing innovative medical devices for interventional cardiology and radiology. Our commitment to excellence in healthcare and patient outcomes drives us to provide the best-in-class stents and balloon catheters. With a growing presence in the global market, we are expanding our team in the...
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Principal Mechanical Engineer – Medical Devices
3 weeks ago
bangalore, India Quest Global Full timeSenior Technical Architect – Medical Devices P- Mechanical Technical Lead – Medical Devices P- Senior Technical Architect – Medical Devices P- Key Responsibilities • Mechanical Design Engineer with 15-20 Years of experience Minimum 8 years’ experience in medical devices, Renal dialysis machines and consumables design . Hands on experience in all...
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iOS SDET – Medical Device Testing
1 week ago
bangalore, India L&T Technology Services Full timeJob Title: iOS SDET – Medical Device Testing Experience: 5+ Years Location: Bangalore Job Description: We are seeking a highly skilled iOS Software Development Engineer in Test (SDET) with a strong background in medical device testing . The ideal candidate will have hands-on experience in automated testing for iOS applications using XCTest/XCUITest with...
