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Strong Tier-1 brand plus a common program manager title increases applicant competition, moderated by senior regulated-role.
Regulated medical-device NPD and design control requirements make industry-specific experience highly important.
Explicit 8–12 years, minimum PM experience, and regulated NPD requirements create stringent shortlisting filters.
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Lead and manage complex New Product Development programs from concept through commercialization within Medical Devices and Laboratory Instruments.
Develop and execute integrated program plans including scope, schedule, resources, milestones, budget, risks, and deliverables, ensuring adherence to quality, regulatory, cost, scope, and schedule commitments.
Drive cross-functional global teams and stakeholder alignment in a matrix organization to ensure timely launches and compliance with Design Control and regulatory requirements.
Bachelor's degree in Engineering or a related technical discipline.
8-12 years of overall industry experience with minimum 5 years in Program Management of complex New Product Development programs.
Experience in regulated product development environments using Phase-Gate or Product Development Lifecycle methodologies.
Work Location: Hyderabad, India (Office environment); PMP certification preferred but not mandatory.
Experienced leader in global, cross-functional program management within regulated medical device or laboratory instrument sectors.
Strong familiarity with Design Control, Risk Management, Change Management, and Product Lifecycle Management processes under regulatory standards.
Data-driven decision maker skilled at managing competing priorities, with expertise in stakeholder influence and program risk management in matrix organizations.