

France-Centre-Val de Loire; Italy-Milan; Spain-Madrid; United Kingdom-Hemel Hempstead
Key Responsibilities:
EDUCATION AND EXPERIENCE
SKILLS AND ATTRIBUTES
משרות נוספות שיכולות לעניין אותך

ADay in the Lifeof the EMEA AI Product Owner:
You’ll begin your day translating business needs into technical requirements, prioritizing features in the backlog, and overseeing the AI product lifecycle to ensure successful, ethical, and valuable implementations. Key responsibilities include defining success criteria, collaborating with data scientists and engineers, and bridging the gap between business goals and AI capabilities.
You will work on initiatives like AgentForce AI, PACE and other new AI opportunities in the region.
You will collaborate with the AI Product Managers, Data Engineering, Platform, Architecture, and Governance teams to clarify data contracts, schemas, lineage, and access models, ensuring each increment is production-ready and guided by design. You’ll groom the roadmap and write user stories to add to the backlog, break down epics, refine acceptance criteria, and balance new features with technical debt, observability, and cost efficiency. You’ll demo recent increments, gather user feedback, and turn it into testable stories that enhance usability, trust, and performance. You’ll brief sponsors on the value delivered and present investment options for the next phases.
Your role is more technically demanding, requiring an understanding of AI technologies and ethical considerations. You must navigate challenges like data privacy and compliance with data protection regulations. Additionally, you will manage AI bias by providing diverse datasets for model training and using bias detection mechanisms to monitor AI outputs.
On a monthly rhythm, you’ll coordinate with global data and architecture forums to reuse patterns, converge on standards, and ensure EMEA needs are represented in the enterprise roadmap.
As a champion of the data strategy & enablement team, you will drive adoption through excellent product experience - discoverability in the catalog, clear documentation, and dependable service levels that help teams selfserve trustworthy, governed data at scale.
The role:
Reporting to the Product Ownership Sr Manager, the EMEA AI Product Owner is accountable for the dayday delivery of data products
You will translate business outcomes into product capabilities, manage scope and trade
Success requires a blend of AI technology expertise, stakeholder leadership, and hands-on ownership to deliver secure, compliant solutions for the EMEA region.
Key Responsibilities:
What you will need:
What do you offer:
What do we offer:
משרות נוספות שיכולות לעניין אותך

As part of the software development team, you will lead the creation of high-performance rendering and workflow tools. You will collaborate closely with hardware engineers, systems engineers, clinical teams, and field technicians to create cutting-edge tools for physicians and care teams. The role will involve full lifecycle software development, including requirements, architecture, design, implementation, and validation.
Your responsibilities will include:
Generate UI concepts and implement prototypes to gather user feedback on workflow and usability
Design and build elegant solutions for complex clinical problems in user interaction and visualization
Lead enhancements for real-time 3D rendering and advanced visualization technology
Collaborate effectively with hardware, systems, quality, and test teams to ensure end-to-end solution integrity
Participate in preclinical system experiments with physicians and third parties to evaluate system performance
Implement, test, troubleshoot, and debug source code for complex medical software applications
Drive software development through the full product lifecycle, including requirements, design, planning, code reviews, and documentation
Contribute to technical documentation such as design specifications, test plans, and user manuals
Foster a culture of pragmatic decision-making and cross-functional collaboration
Identify and drive continuous improvements in development tools and processes
Support field clinical staff with software use and issue troubleshooting
Required Qualifications:
BS or MS in Computer Science or a related field
Minimum of 5 years' experience in software development
Strong programming experience in C++
Experience with OpenGL and 3D graphics programming
Solid understanding of object-oriented programming principles
Excellent analytical and problem-solving skills
Demonstrated ability to understand user needs and design intuitive user interfaces
Ability to manage multiple projects in parallel
Experience with full software development lifecycle processes
Strong communication skills, both written and verbal
Preferred Qualifications:
Experience with Qt (QML is a plus)
Experience developing on Linux platforms
Familiarity with Agile and Scrum methodologies
Understanding of medical device standards such as IEC 62304, IEC 60601, ISO 14971, ISO 13485
Experience with software tools such as Git, Jira, and JAMA
Experience mentoring junior engineers
Quick learner with adaptability to master complex systems and new technologies
Working conditions:
Hybrid work model
Travel: 0–10%
Maximum Salary: $ 197000
Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions: It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
Among other requirements, Boston Scientific maintains specific prohibited substance test requirements for safety-sensitive positions. This role is deemed safety-sensitive and, as such, candidates will be subject to a prohibited substance test as a requirement. The goal of the prohibited substance testing is to increase workplace safety in compliance with the applicable law.
משרות נוספות שיכולות לעניין אותך

ADay in the Lifeof the EMEA AI Product Owner:
You’ll begin your day translating business needs into technical requirements, prioritizing features in the backlog, and overseeing the AI product lifecycle to ensure successful, ethical, and valuable implementations. Key responsibilities include defining success criteria, collaborating with data scientists and engineers, and bridging the gap between business goals and AI capabilities.
You will work on initiatives like AgentForce AI, PACE and other new AI opportunities in the region.
You will collaborate with the AI Product Managers, Data Engineering, Platform, Architecture, and Governance teams to clarify data contracts, schemas, lineage, and access models, ensuring each increment is production-ready and guided by design. You’ll groom the roadmap and write user stories to add to the backlog, break down epics, refine acceptance criteria, and balance new features with technical debt, observability, and cost efficiency. You’ll demo recent increments, gather user feedback, and turn it into testable stories that enhance usability, trust, and performance. You’ll brief sponsors on the value delivered and present investment options for the next phases.
Your role is more technically demanding, requiring an understanding of AI technologies and ethical considerations. You must navigate challenges like data privacy and compliance with data protection regulations. Additionally, you will manage AI bias by providing diverse datasets for model training and using bias detection mechanisms to monitor AI outputs.
On a monthly rhythm, you’ll coordinate with global data and architecture forums to reuse patterns, converge on standards, and ensure EMEA needs are represented in the enterprise roadmap.
As a champion of the data strategy & enablement team, you will drive adoption through excellent product experience - discoverability in the catalog, clear documentation, and dependable service levels that help teams selfserve trustworthy, governed data at scale.
The role:
Reporting to the Product Ownership Sr Manager, the EMEA AI Product Owner is accountable for the dayday delivery of data products
You will translate business outcomes into product capabilities, manage scope and trade
Success requires a blend of AI technology expertise, stakeholder leadership, and hands-on ownership to deliver secure, compliant solutions for the EMEA region.
Key Responsibilities:
What you will need:
What do you offer:
What do we offer:
משרות נוספות שיכולות לעניין אותך

DEIN VERANTWORTUNGSBEREICH
DEIN KOMPETENZPROFIL
משרות נוספות שיכולות לעניין אותך

Your responsibilities will include:
Required qualifications:
Preferred qualifications:
Compensation fornon-exempt (hourly), non-sales rolesmay also include variable compensation from time to time (e.g., any overtime and shift differential) and annual bonus target (subject to plan eligibility and other requirements).
Compensation forexempt, non-sales rolesmay also include variable compensation, i.e., annual bonus target and long-term incentives (subject to plan eligibility and other requirements).
For MA positions:It is unlawful to require or administer a lie detector test for employment. Violators are subject to criminal penalties and civil liability.
Please be advised that certain US based positions, including without limitation field sales and service positions that call on hospitals and/or health care centers, require acceptable proof of COVID-19 vaccination status. Candidates will be notified during the interview and selection process if the role(s) for which they have applied require proof of vaccination as a condition of employment. Boston Scientific continues to evaluate its policies and protocols regarding the COVID-19 vaccine and will comply with all applicable state and federal law and healthcare credentialing requirements. As employees of the Company, you will be expected to meet the ongoing requirements for your roles, including any new requirements, should the Company’s policies or protocols change with regard to COVID-19 vaccination.
משרות נוספות שיכולות לעניין אותך

Belgium-Diegem; France-Voisins le Bretonneux; Germany-Düsseldorf; Italy-Milan; Netherlands-Kerkrade; Spain-Madrid; United Kingdom-Hemel Hempstead
About the role:
This is a highly dynamic role in which you will work in a team environment to develop global evidence-based clinical strategies for cardiology medical devices (Cardiac Rhythm Management) by creating clinical documentation that systematically synthesizes information from multiple data sources. As a Clinical Evaluation Scientist, you will plan and develop clinical evaluation reports (CERs) and post-market clinical follow-up (PMCF) reports, as well as summary of safety and clinical performance reports (SSCPs) in alignment with applicable clinical and regulatory standards and business needs. This role applies analytical thought processes and a highly methodical clinical evaluation approach to develop benefit/risk profiles for the Boston Scientific portfolio cardiology devices. A successful candidate has excellent writing skills as well as the ability to work collaboratively with cross-functional partners. Your efforts support product approval, indication expansion and claim support, and mandated post-market requirements.
Your responsibilities will include:
Compile, appraise, and evaluate data from multiple sources including clinical trials, medical literature, design verification/validation data, and product complaint data. Compare and align this data with Risk Documentation and product labeling to identify gaps or emergent concerns.
Develop literature search strategies in collaboration with librarians and perform methodical evaluation of medical literature including screening, appraisal and extraction of relevant data.
Develop Clinical Benefit Statements in collaboration with medical experts and develop pre- and post-market data collection strategies to support the developed statements.
Create analyses to evaluate product benefit/risk profile, safety (e.g., develop a profile of adverse events), and performance. Identify potential clinical evidence gaps and contribute to development of prospective evidence strategy to address gaps.
Develop global clinical data strategies in collaboration with leadership and cross-functional partners to support market access for New Product Development, Sustaining Product compliance and Design Changes to existing products.
Manage ongoing Design and Quality activities to support necessary changes and/or improvements to devices, including assessing the impact to existing clinical data strategies, proposing and developing new clinical data activities to meet any identified gaps, and coordinating with management to ensure resourcing needs are considered.
Aid in the development and execution of strategies for responses for regulatory submissions.
Minimum Qualifications
Bachelor’s, Master’s or Advanced degree (PhD, research-based MS, MD, RN, DVM) in a scientific, medical, or engineering field.
6+ years professional experience in a scientific, engineering, medical, or medical device space
3+ years of experience inat least oneof the following: 1) Writing and Developing Clinical Evaluation Plans/Reports and Post-Market Clinical Follow-Up Plans/Reports in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations), relevant Medical Device Coordination Group (MDCG) guidance, and harmonized standards; 2) Working in the clinical treatment and management of patients receiving Cardiac Rhythm Therapies, including but not limited to: Pacemakers; Implantable Cardioverter-Defibrillators (ICDs); Cardiac Resynchronization Therapy Pacemakers/Defibrillators (CRT-P/Ds); or Subcutaneous Implantable Cardioverter Defibrillators (S-ICDs) or 3) Writing, Developing, Managing, and Submitting Regulatory Technical Documentation submissions in accordance with Regulation (EU) 2017/745 of the European Parliament (i.e., EU Medical Device Regulations) to support EU Market access of Cardiac Rhythm Devices
Thorough understanding of different types of clinical evidence (e.g., literature, clinical trials, real-world evidence, etc.) and the benefits and limitations of each type of data.
Experience in strategically applying knowledge of regulations, medical knowledge, and data types to develop clinical data strategies to support submission.
Analytical skills, including strong familiarity with medical literature
Strong medical/scientific writing skills
Preferred Qualifications
3+ years of professional experience inmultipleof the areas identified above
Experience with/knowledge of with Quality Management System documentation, specifically Risk Management Documents (e.g., Hazard Analysis, Risk Management Report, Risk Management Plan)
Experience with engineering documentation, including test protocols, test reports, and international standards
משרות נוספות שיכולות לעניין אותך

France-Centre-Val de Loire; Italy-Milan; Spain-Madrid; United Kingdom-Hemel Hempstead
Key Responsibilities:
EDUCATION AND EXPERIENCE
SKILLS AND ATTRIBUTES
משרות נוספות שיכולות לעניין אותך