Medtronic

Healthcare

EngineeringProgramManager

₹60–90L ~AI est. Hyderabad, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Engineering Program Manager at Medtronic. Skills: Program management, Software development, Regulatory compliance. Lead planning and execution of large, cross-functional engineering. Translate therapy strategy and business priorities into integrated,”

What You'll Achieve.

Balance speed, quality, compliance, and business outcomes

Industry & Context.

Healthcare
Problems you'll solve

Risk management; Trade-offs; Root cause analysis

Eligibility Requirements

Travel up to 25%

What They're Looking For.

Must Have

Bachelor's degree in Engineering, Computer Science, or related discipline, 18+ years of overall experience, 8+ years in engineering or program management leadership within regulated product development, 5+ years of early career hands on Software Engineering/Development experience, Deep experience with software and systems development in medical devices or similarly regulated industries, working knowledge of IEC 62304, ISO 14971, Design Controls, and FDA regulations, Demonstrated success leading complex, software-enabled medical device programs with significant regulatory and patient risk, influencing skills across global and matrixed organizations, Proven ability to balance speed, quality, compliance, and business outcomes, Experience mentoring senior talent and shaping program management best practices

Nice to Have

Master's degree (Engineering, MBA, or related), PMP certification, Experience with Microsoft Project, ProChain, or advanced scheduling methodologies, Prior exposure to Neuromodulation, Pelvic Health, implantable devices, or therapy platforms, Exposure to digital, analytics, or AI-enabled capabilities within regulated product development environments

What You'll Do.

Lead planning and execution of large

cross-functional engineering

Translate therapy strategy and business priorities into integrated

Drive program governance

Make program decisions aligned to regulatory standards

Ensure integration of Quality and Regulatory partners

Own complex dependency management across teams

Lead design readiness reviews

Lead milestone reviews

Lead design transfer to operations

Ensure documentation completeness

Ensure manufacturing readiness

Proactively identify risks

Proactively identify trade-offs

Escalate risks and trade-offs with clarity and recommendations

Provide executive-level communication on program status

Provide executive-level communication on program risks

Provide executive-level communication on strategic implications

Lead senior cross-functional stakeholders

Influence senior cross-functional stakeholders

Own integrated schedules

Own resource strategies

Own delivery commitments

Act as a trusted execution partner

Support portfolio prioritization through data-driven insights

Support portfolio prioritization through lessons learned

Mentor program managers

Mentor technical leads

Raise execution maturity across teams

Provide functional leadership to program teams

Provide functional leadership to vendors

Mentor junior program managers

Elevate delivery excellence

How You'll Work.

Team & Collaboration

Cross-functional engineering programs; Cross-functional stakeholders; Global and matrixed organizations; R&D, Quality, Regulatory, Clinical, Operations, and Supply Chain

Communication Scope

Executive-level communication; Clarity and recommendations

Process & Methodology

Program management, Agile, Scrum, Roadmap planning, Kanban, PMP

Full Job Description

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world. # **A Day in the Life** The Engineering Program Manager will provide senior-level program leadership across Neuromodulation and Pelvic Health portfolios, owning end-to-end delivery of software-intensive programs across multiple releases or platforms. The role requires strong judgment, influence, and execution maturity in highly regulated environments. **Responsibilities may include the following and other duties may be assigned:** * Lead planning and execution of large, cross-functional engineering programs supporting Neuromodulation and Pelvic Health therapy platforms. * Translate therapy strategy and business priorities into integrated, executable program plans across software, systems, firmware, and hardware. * Drive program governance, risk management, and decision-making aligned to FDA and global regulatory standards, including IEC 62304, ISO 14971, and Design Controls. * Ensure early and sustained integration of Quality and Regulatory partners throughout the development lifecycle. * Own complex dependency management across teams, suppliers, and global sites. * Lead design readiness, milestone reviews, and design transfer to operations, ensuring compliance, documentation completeness, and manufacturing readiness. * Proactively identify risks, trade-offs, and mitigation strategies; escalate with clarity and recommendations. * Provide executive-level communication on program status, risks, and strategic implications. * Lead and influence senior cross-functional stakeholders across R&D, Quality, Regulatory, Clinical, Operations, and Supply Chain. * Own integrated schedules, resource strategies, and delivery commitments aligned to therapy and portfolio objectives. * Act as a trusted execution partner to OU and MEIC leadership.

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