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Tier-1 brand, mid-level PM, metro location, and generalist cross-functional requirements increase competition.
High because regulated medical device compliance and healthcare product experience are critical and less transferable.
Mandatory 5+ years, engineering degree and healthcare product experience enforce strict shortlisting.
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Lead and manage software-intensive programs in regulated medical device environments from initiation to product launch.
Ensure cross-functional alignment among software, systems, firmware engineering, Quality, Regulatory Affairs, Manufacturing, and Product Management teams for seamless program execution.
Maintain quality and compliance by adhering to organizational quality management systems and policies.
Bachelor's degree in Computer Science or equivalent Engineering degree (B.E).
Minimum 5 years of relevant Project Management experience in healthcare product environment.
Experience with medical device design controls, secure product development, and software release/deployment practices.
Onsite work location: Bengaluru, India; flexible to align with Sweden and Sunnyvale team timings as needed.
Experienced in leading complex programs in regulated healthcare or life sciences product development.
Skilled in cross-functional coordination across engineering, quality, regulatory, manufacturing, and product teams.
Certified in project management frameworks such as PMP or Agile (Scrum/SAFe) to effectively drive projects.