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Medical Devices Regulatory jobs
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- Tacticity AdvisorsPune, Maharashtra
- Work directly with the founder on FDA submissions for medical devices.
- Who Should Apply * Hands-on experience in medical device regulatory affairs is required.
- Tacticity AdvisorsPune, Maharashtra
- Work directly with the founder on FDA submissions for medical devices.
- Who Should Apply * Past hands-on work with medical devices (job or internship) in…
- Siemens HealthineersGurugram, Haryana
- Support business partners in zone countries like Bangladesh, Sri Lanka, Nepal, Maldives & Bhutan to comply regulatory requirements related to Medical devices…
- Clarity medical pvt ltdChandigarh
- Lead Product Quality and Quality Assurance activities for medical devices.
- Ensure compliance with applicable *MDR 2017, CDSCO and medical-device regulatory…
- Siemens HealthineersBengaluru, Karnataka
- You will provide professional advice to and actively support internal departments, such as product management, (clinical) marketing- and product development in…
- OrcapodPune, Maharashtra
- Experience with Medical device testing or knowledge of relevant regulatory standards (FDA, ISO 13485) is a plus.
- Experience with version control systems.
- Plebc Innovations Private LimitedGachibowli, Hyderabad, Telangana
- Basic understanding of medical devices and their development lifecycle.
- Hands-on experience in medical device regulatory affairs.
View similar jobs with this employerMasimoRemote in Bengaluru, Karnataka- Knowledge of regulatory submission requirements for India Class II medical devices.
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- PfizerVisakhapatnam, Andhra Pradesh
- Experience with regulatory queries and responses.
- Support preparation and review of technical documentation and responses for regulatory submissions and…
- Fresenius Medical CareBengaluru, Karnataka
- Lead regulatory aspects of product and process changes, including regulatory documentation.
- Experience with cybersecurity, data protection (GDPR), and cloud…
- U Square Lifescience Pvt. Ltd.Ahmedabad, Gujarat
- Technical query response to the various regulatory authorities.
- Dossier preparation as per the ACTD & CTD (Module I, II, III, IV and V) guideline.
- Digi VitalsNoida, Uttar Pradesh
- Coordinate regulatory and certification activities related to CDSCO, medical device licensing, and applicable documentation.
- Medpace, Inc.Navi Mumbai, Maharashtra
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
- Medpace, Inc.Navi Mumbai, Maharashtra
- Medpace is a full-service clinical contract research organization (CRO) providing phase l-lV clinical development services to the biotechnology, pharmaceutical,…
- MedtronicNanakramguda, Hyderabad, Telangana
- Review change control documents and ascertain regulatory impact for external and internal documents through formal regulatory assessments.
- Navitas Life SciencesBengaluru, Karnataka
- Provide QA consultancy to project teams on regulatory requirements, guidelines, and SOPs, as required.
- Conduct audits of projects, systems, processes, and…
Job Post Details
Regulatory Affairs – Medical Devices (Full-Time)
Tacticity Advisors
Pune, Maharashtra
₹50,000 - ₹1,00,000 a month
-
Full-time
Regulatory Affairs – Medical Devices (Full-Time)
Tacticity Advisors
•
Pune, Maharashtra
•
₹50,000 - ₹1,00,000 a month
Job details
₹50,000 - ₹1,00,000 a month
Full-time
Pune, Maharashtra
Full job description
Regulatory Affairs – Medical Devices (Full-Time)
Work directly with the founder on FDA submissions for medical devices. You will research regulatory pathways, review test data, help draft parts of submissions and join client calls.
Who Should Apply • Hands-on experience in medical device regulatory affairs is required. Work on an FDA submission (510(k), De Novo or PMA) is a plus. • Well spoken in English, outspoken and confident with new people • Eager to learn and open to feedback • Degree in Life Sciences, Biomedical Engineering, Biotechnology, Pharmacy or Engineering
What You Will Gain • Learn how medical devices get approved by the U.S. FDA, from a former FDA reviewer • Hands-on submission work and real client exposure • Room to grow with the company as it expands Details Full-time role | Office in Balewadi, Pune
How to Apply Email your CV to: hr@tacticityadvisors.com
Subject: Application – Regulatory Affairs – Full-Time
Pay: ₹50,000.00 - ₹100,000.00 per month
Work Location: In person
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