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EBU IT Business Partner
Company | Analog Devices |
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Location | Burlington, MA, USA |
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Salary | $144000 – $198000 |
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Type | Full-Time |
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Degrees | Bachelor’s, MBA |
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Experience Level | Expert or higher |
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Requirements
- 15+ years experience in IT or digital roles within the medical device, medtech, or regulated healthcare environment
- Demonstrated experience in business partnering or digital transformation leadership roles in cross-functional settings
- Strong knowledge of medical device lifecycle, including product development, regulatory submissions, and commercial launch
- Excellent facilitation and communication skills with ability to lead strategy sessions, build consensus, and drive alignment
- Proven program delivery track record in matrixed organizations with complex stakeholder environments
- Bachelor’s degree required; advanced degree (MBA, MS in Engineering, etc.) preferred
Responsibilities
- Act as the single point of contact (SPOC) between EBU leadership and CIO org for all digital and IT-related initiatives
- Lead strategy facilitation sessions to align all stakeholders (engineering, regulatory, quality, legal, product security, commercial) on the medical device lifecycle roadmap
- Translate EBU business strategies into IT and digital roadmaps, ensuring prioritization of value-driving use cases
- Drive and manage cross-functional programs that span ideation, design, regulatory readiness, clinical, and go-to-market
- Oversee execution of digital enablers (e.g., product lifecycle systems, QMS, design control systems, secure device connectivity, data platforms)
- Partner with legal, compliance, cybersecurity, and product security to ensure risk-aware execution across global medical regulatory landscapes
- Collaborate with enterprise architects, data engineers, and cybersecurity leads to ensure fit-for-purpose architectures for regulated devices
- Ensure data governance, privacy, and security best practices are integrated into product development workflows
- Support integration of real-world data, post-market surveillance tools, and digital services into product strategies
Preferred Qualifications
- Familiarity with design control, DHF, QMS, ISO 13485, 21 CFR Part 820, and related standards
- Experience with digital health, connected medical devices, or real-world evidence platforms
- Ability to operate with executive presence and influence across business and technical teams