• Serve as the primary Subject Matter Expert for Quality and Regulatory Affairs across medical device product lines, providing strategic guidance to internal teams and clients.
• Architect end-to-end regulatory solutions for complex client problem statements, translating business needs into actionable regulatory strategies.
• Lead the design and development of winning solutions, proposals, and customer-facing presentations in response to RFPs, RFIs, and strategic business opportunities.
• Define and drive go-to-market (GTM) strategy for quality and regulatory service offerings, identifying new business opportunities and market positioning.
• Partner with sales, pre-sales, and delivery teams to craft differentiated value propositions and win themes for regulatory consulting engagements.
• Advise clients on regulatory submission strategies, including 510(k), PMA, De Novo, EU MDR technical documentation, and emerging requirements under the EU AI Act.
• Monitor and interpret evolving regulatory requirements across FDA (US), EU MDR/IVDR, PMDA (Japan), CDSCO (India), NMPA (China), and other major geographies, translating changes into actionable guidance.
• Support clients through the full product lifecycle – from regulatory classification and strategy through submission, approval, and post-market surveillance.
• Build and mentor internal regulatory capability, establishing best practices, templates, and playbooks for proposal development and client delivery.
• Represent the organization in client discussions, workshops,



and industry forums as a thought leader in medical device quality and regulatory affairs.
• Collaborate with cross-functional teams (Quality, Clinical, Engineering, Legal) to ensure proposed solutions are technically sound and compliant. Required Skills & Experience
• 15–20 years of progressive experience in Quality and Regulatory Affairs within the medical device industry.
• Proven track record of creating winning solutions, proposals, and customer presentations for regulatory consulting or managed-services engagements.
• Extensive, hands-on experience with global regulatory frameworks, including:
• US FDA – 510(k), PMA, De Novo pathways
• European Union – EU MDR, EU IVDR, and the EU AI Act
• Japan – PMDA requirements and approval processes
• India – CDSCO regulations
• China – NMPA regulations, and other emerging geographies
• Deep expertise in quality management systems (ISO 13485, ISO 14971) and their application to regulatory submissions.
• Demonstrated ability to architect solutions for complex, multi-geography regulatory problem statements.
• Solid experience responding to complex RFPs – including solution design, pricing strategy input, and executive-level storytelling.
• Excellent client-facing communication, presentation, and negotiation skills, with experience engaging C-suite and senior stakeholders.
• Strong business acumen with the ability to connect regulatory strategy to commercial outcomes and go-to-market planning.
• Experience mentoring teams and building organizational regulatory capability and thought leadership.

📌 Quality and Regulatory Practice Leader (Bengaluru)
🏢 Cyient
📍 Bengaluru