

Senior Sourcing Specialist – I.T.
Responsible for developing and executing sourcing strategies for theInformation Technology Category.
Responsibilities:
Support the Information Technology Category Team with sourcing of I.T. Software, Hardware, and Services.
Contribute to the development and implementation of I.T. Sourcing Strategies that align with business objectives and drive cost savings
Support development of the Annual Clinical Category Plan via research, analytics, and development of presentation materials.
Lead Sourcing Events for the I.T. Category: RFQ, RFP, RFI and Auctions.
Facilitate overall supplier selection process, including analysis of proposals, development of recommendations, and facilitation of decision-making process.
Negotiate and drive towards the execution of contracts with existing and new service providers. Detailed contract review and editing expected.
Conduct benchmarking projects and analysis to determine best in class opportunities. Develop cost modelling and business cases.
Report accomplishments and communicate project status and critical issues to I.T. and Sourcing Leadership.
Responsible for driving and tracking cost reductions to meet business targets.
Maintain and support vendor contracts and databases.
Organize and participate in Supplier Business Reviews.
Support continuous improvement of Procurement Processes (Sourcing & Purchasing).
Ensure compliance with the Boston Scientific Quality System and Approved Vendor List
Negotiate favorable payment terms with suppliers
While based in EMEA, the scope will include local and global vendors
Required Qualifications:
Bachelor's degree in Business, Computer Science, Engineering or related field
4-6 years’ experience within I.T. or related Sourcing/Procurement functions
Ability to work independently, lead Sourcing events and interact with stakeholders to meet customer requirements and deliver savings.
Demonstrated project management skills; ability to effectively manage multiple tasks/projects simultaneously
Strong interpersonal skills with the ability to interface with suppliers and employees
Strong analytical skills for data analysis and reporting
Excellent communication and presentation skills
Proficiency in MS Office Applications (Excel, PPT, Word, etc.)
Experience with contracts drafting
Fluent in English
Available to travel within EMEA.
Desired Qualifications:
IT systems knowledge in SAP, Ariba or similar Sourcing / Procurement Suites
Market and legal knowledge required in addition to procurement skills
Experience with SaaS agreements, Hardware, and Software contracts
What we offer:
A competitive compensation and benefits package
Working in an international environment
Possibility to make an impact
Fast Growing and innovative environment
Language courses
Free and confidential counselling support/program (Psychological, Financial, Legal)
Parental leave policy
Medical Care (Premium Package)
Life insurance
Lunch Card
Employee Stock Purchase Plan
Employee Savings Plan
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About the role:
This position is responsible for the strategic planning and execution of PI Vascular Medical Affairs and Professional Education meetings.
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.
So, choosing a career with Boston Scientific (NYSE: BSX) isn’t just business, it’s personal. And if you’re a natural problem-solver with the imagination, determination, and spirit to make a meaningful difference to people worldwide, we encourage you to apply and look forward to connecting with you!
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

Purpose Statement
The General Accounting Process Steward plays a pivotal role in leading and executing transformation initiatives within the Accounting (ATR) organization. Reporting to the Global Process Leader (GPL), this position is responsible for advancing the global accounting change agenda and driving the process improvement roadmap across all General Accounting processes.
1. End-to-End Process Expertise & Value Improvement
2. Global Process Leader (GPL) Roadmap Support
3. Change Leadership
4. Performance Measurement & Continuous Improvement
5. Governance & Risk Management
Qualifications
Quality Requirements
What We Offer
משרות נוספות שיכולות לעניין אותך

Key Responsibilities:
What are we looking for in you?
We offer:
משרות נוספות שיכולות לעניין אותך

About the Role
You will collaborate with internal teams, external advisors, and tax authorities, gaining hands-on experience with VAT reporting processes in an international and dynamic environment.
Key Responsibilities
Qualifications
What We Offer
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

Key Responsibilities:
Qualifications:
What We Offer
משרות נוספות שיכולות לעניין אותך

Senior Sourcing Specialist – I.T.
Responsible for developing and executing sourcing strategies for theInformation Technology Category.
Responsibilities:
Support the Information Technology Category Team with sourcing of I.T. Software, Hardware, and Services.
Contribute to the development and implementation of I.T. Sourcing Strategies that align with business objectives and drive cost savings
Support development of the Annual Clinical Category Plan via research, analytics, and development of presentation materials.
Lead Sourcing Events for the I.T. Category: RFQ, RFP, RFI and Auctions.
Facilitate overall supplier selection process, including analysis of proposals, development of recommendations, and facilitation of decision-making process.
Negotiate and drive towards the execution of contracts with existing and new service providers. Detailed contract review and editing expected.
Conduct benchmarking projects and analysis to determine best in class opportunities. Develop cost modelling and business cases.
Report accomplishments and communicate project status and critical issues to I.T. and Sourcing Leadership.
Responsible for driving and tracking cost reductions to meet business targets.
Maintain and support vendor contracts and databases.
Organize and participate in Supplier Business Reviews.
Support continuous improvement of Procurement Processes (Sourcing & Purchasing).
Ensure compliance with the Boston Scientific Quality System and Approved Vendor List
Negotiate favorable payment terms with suppliers
While based in EMEA, the scope will include local and global vendors
Required Qualifications:
Bachelor's degree in Business, Computer Science, Engineering or related field
4-6 years’ experience within I.T. or related Sourcing/Procurement functions
Ability to work independently, lead Sourcing events and interact with stakeholders to meet customer requirements and deliver savings.
Demonstrated project management skills; ability to effectively manage multiple tasks/projects simultaneously
Strong interpersonal skills with the ability to interface with suppliers and employees
Strong analytical skills for data analysis and reporting
Excellent communication and presentation skills
Proficiency in MS Office Applications (Excel, PPT, Word, etc.)
Experience with contracts drafting
Fluent in English
Available to travel within EMEA.
Desired Qualifications:
IT systems knowledge in SAP, Ariba or similar Sourcing / Procurement Suites
Market and legal knowledge required in addition to procurement skills
Experience with SaaS agreements, Hardware, and Software contracts
What we offer:
A competitive compensation and benefits package
Working in an international environment
Possibility to make an impact
Fast Growing and innovative environment
Language courses
Free and confidential counselling support/program (Psychological, Financial, Legal)
Parental leave policy
Medical Care (Premium Package)
Life insurance
Lunch Card
Employee Stock Purchase Plan
Employee Savings Plan
משרות נוספות שיכולות לעניין אותך