Posted:4 hours ago|
Platform:
Work from Office
Full Time
We are seeking an experienced and strategic VP of Software Engineering to lead our Software teams in the India Development Center (IDC) to develop and maintains the IDC to become a R&D organization that delivers software solutions and sustain Cepheid Software products and strategical objectives, through a team of leaders and associates in the IDC. The role, directs and implements strategies and initiatives to maximize site value creation for Cepheid Software teams.
This position is a leadership role, reports to Vice President, R&D and is part of the Software Engineering within Global R&D and will be located at Bangalore, India.
In this role, you will have the opportunity to:
The essential requirements of the job include:
Minimum 10 years of experience in software development leadership within regulated industries such as medical device manufacturing, including direct application of ISO 13485 and IEC 62304 standards, with a bachelors or masters degree in engineering, computer science, or related field
Proven track record of managing site-level software engineering operations, including budget oversight, resource allocation, and delivery of software releases aligned with strategic business objectives
Demonstrated expertise in implementing and monitoring engineering KPIs, OKRs, and performance metrics through structured programs and reporting systems across cross-functional teams
Minimum 5 years of experience leading technical planning and execution for software teams, including coordination of technical presentations, stakeholder negotiations, and strategic roadmap alignment
Experience recruiting, retaining, and performance-managing R&D staff in high-compliance environments, including execution of topgrading strategies and succession planning
Direct experience driving engineering excellence across quality, security, performance, and resilience domains, with measurable outcomes in product lifecycle and release management
Hands-on experience with medical software development lifecycle tools and systems, including LIMS, ELN, used in FDA- and ISO-regulated environments
It would be a plus if you also possess previous experience in:
Proven track record of building and leading larger teams, lead multiple high priority programs in a fast paced environment
Experience overseeing departmental P&L ownership exceeding $10M annually, including budget planning, cost optimization, and financial reporting
5+ years of experience in regulated industries such as medical devices, diagnostics, or biotech, with working knowledge of FDA, ISO 13485, and CAP/CLIA compliance frameworks
Demonstrated strong ability in business acumen, grasp big picture and explain to the teams in simple terms
Demonstrated ability to implement scalable team structures and performance metrics using OKRs, KPIs, and structured feedback systems across multi-site operations
Cytiva
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