10 дней назад
Senior Principal Product Manager (Medtech)
102 720 - 154 080€
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Senior Principal Product Manager (Medtech): Defining and delivering connected cardiac-care products across device, cloud, mobile, and enterprise solutions with an accent on patient outcomes, interoperability, safety, and regulatory compliance. Focus on leading continuous discovery, prioritizing complex backlogs, managing device and digital lifecycles, and translating AI/ML capabilities into safe clinical product requirements.
Location: Hybrid role in Galway, County Galway, Ireland
Salary: €102,720–€154,080 per year, plus eligibility for the Incentive Plan.
Company
develops healthcare technologies, including connected cardiac-care solutions that help clinicians monitor and manage patients with implantable cardiac devices.
What you will do
- Define product vision and roadmaps for connected device, cloud, mobile, and enterprise solutions based on patient and clinician workflows.
- Lead continuous discovery with patients, clinicians, and care teams, converting evidence and post-market signals into product opportunities and delivery priorities.
- Own product KPIs, outcome-based OKRs, prioritization frameworks, and the end-to-end backlog, including problem statements, acceptance criteria, and value hypotheses.
- Make trade-off decisions across safety, reliability, quality, scope, time, cost, technology, and technical debt.
- Manage the full device and digital product lifecycle, including modernization, obsolescence planning, phase-in/phase-out activities, launch readiness, and supply continuity.
- Partner with engineering, quality, regulatory, security, operations, commercial, clinical, and executive stakeholders, and accept delivered work against safety, regulatory, and quality criteria.
Requirements
- Honours Bachelor’s degree and at least 10 years of product management experience, or equivalent, including direct backlog ownership and delivery accountability.
- Experience managing regulated, safety-critical, global device and digital products, roadmaps, outcomes, and prioritized backlogs.
- Experience working in Agile environments with epics, stories, acceptance criteria, sprint ceremonies, and formal increment acceptance.
- Strong ability to lead cross-functional teams by influence and make evidence-based product and investment trade-offs.
- Fluency across software platforms such as cloud, mobile, and enterprise systems and/or embedded systems.
- Ability to evaluate AI/ML capabilities and translate them into strategic product requirements while maintaining safety, regulatory compliance, and clinical standards.
Nice to have
- Experience with FDA, EU MDR, and ISO 13485 frameworks, design reviews, risk assessments, and audit interactions.
- Experience embedding cybersecurity, privacy, reliability, and safety-by-design principles into product architecture and backlogs.
- Experience with business cases, P&L influence, ROI modeling, and multi-year investment decisions.
- Experience with continuous discovery, empowered teams, platform strategies, API ecosystems, and interoperability standards such as FHIR.
- Understanding of AI-enabled care delivery and regulatory or reimbursement frameworks for AI/ML as a medical device.
Culture & Benefits
- Mission-driven work focused on improving patient outcomes through healthcare technology.
- Global collaboration across product, engineering, clinical, regulatory, quality, security, operations, and commercial functions.
- Hybrid work arrangement in Galway.
- Flexible benefits package and competitive compensation.
- Short-term incentive eligibility through the Incentive Plan.
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