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Tier-1 brand, product title, and metro location increase applicant competition despite seniority and niche medtech focus.
Strong medical-device and regulatory requirements limit cross-industry transferability of candidate experience.
Mandatory 10+ years and medical-device/regulatory expertise significantly tighten candidate filters.
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Accountable for end-to-end lifecycle management of the Sleep therapy global portfolio, including product development, launch, maintenance, and market release.
Drive portfolio optimization by evaluating legacy products for rationalization and growth opportunities to ensure sustained global market success.
Lead cross-functional teams and create sales enablement, training, and marketing assets to align products with customer needs and regulatory compliance.
10+ years experience in product management, marketing, or related commercial/strategic roles in medical devices or health technology within an international business environment.
Bachelor's or Master’s degree in Business Administration, Marketing, Engineering, Product Management, or equivalent.
Experience delivering complex projects meeting features, cost, quality, and launch targets.
Ability to travel >25% domestically and globally and work in-office at least three days per week in Pune, India location.
Experienced in managing global medical device product lifecycles with strong expertise in market research, regulatory frameworks (FDA, EU MDR), and reimbursement considerations.
Skilled in strategic planning, stakeholder management, and leading cross-disciplinary discussions in a global matrix organization.
Capable of acting as a subject matter expert and voice of the customer to influence product roadmap and portfolio decisions.