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Tier-1 employer and metro location increase competition, but senior 12+ years reduces applicant density.
Highly domain-specific medical-device engineering and regulatory requirements limit cross-industry transferability.
Explicit 12+ years, engineering background, and regulated medical-device experience raise strict screening standards.
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Lead and execute large-scale projects driving global sourcing strategies including supplier management, product launch, and lifecycle management.
Manage project scope, technical and risk assessment, develop WBS, RACI, effort estimation, and ensure achievement of key milestones including cost, quality, and delivery targets.
Drive cross-functional collaboration, stakeholder management, business case development, risk mitigation, and ensure compliance with corporate and regulatory policies.
Bachelor’s or Master’s degree in Mechanical, Electrical, Electronics Engineering or equivalent.
12+ years of experience in high-tech industry focusing on mechanical or electrical/electronics engineering design.
Experience in project management with capability to lead teams and influence cross-functional stakeholders.
Role is office-based; full-time onsite presence required at company facilities.
Experienced in managing complex engineering projects with solid understanding of supplier, product lifecycle, and change management.
Familiarity with project management tools such as MS Project, Smartsheets, Power BI and methodologies like Lean and Design for Excellence.
Strong business acumen with experience in business case development, cost optimization, and stakeholder engagement in regulated environments (medical device domain preferred).