Regulatory Specialist Lead- Medical Devices (India)

Regulatory Specialist Lead- Medical Devices (India)

13 Aug
|
Cyient
|
India

13 Aug

Cyient

India

Senior Regulatory Affairs skilled with 8+ years of experience in medical devices, specializing in US FDA, EU MDR, and APAC regulations.
Proven track record in leading 510(k), PMA, and EU Technical Documentation submissions, managing audits and inspections, and driving end-to-end regulatory compliance across the product lifecycle.
Strong cross-functional collaborator, experienced in global stakeholder engagement, regulatory strategy, post-market surveillance, and mentoring teams in complex, multi-market environments.
Experience required : 8 to 12 years
Location : Pune.
To succeed in this role, you should have the following skills and experience:
MS or PhD in relevant field including Computer, Electrical, Mechanical Engineering, or other related science.
A minimum of 8 to 12 years of experience successfully developing complex medical devices (hardware, software, consumables) products for acute care/hospital markets is necessary.
Hands-on experience (technical) in ventilation is a plus.
Knowledge of Statistical Data Analysis is necessary.



Includes ability to critically evaluate proposed study designs with basic knowledge of statistics, the calculation of sample sizes and/or estimation of statistical power.
Experience with conducting cross-discipline feasibility and trade off studies to evaluate electronic, mechanical, and pneumatic performance from subsystem to system level for issue resolutions
Solid understanding of System Verification and Validation test plan/protocols, executing V&V; activities, generating, and analyzing test reports
Understanding of global medical device regulatory environments and clearance processes.
Effective communication, documentation, presentation, and interpersonal skills are required, as well as the ability to work both independently and as part of a team.
Experience auditing a DHF (Design History File - a compilation of records which describe the design history of a finished device) for compliance with internal processes and external

📌 Regulatory Specialist Lead- Medical Devices (India)
🏢 Cyient
📍 India

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