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דרושים Field Managed Care Specialist ב-Boston Scientific ב-United States, Marlborough

מצאו את ההתאמה המושלמת עבורכם עם אקספוינט! חפשו הזדמנויות עבודה בתור Field Managed Care Specialist ב-United States, Marlborough והצטרפו לרשת החברות המובילות בתעשיית ההייטק, כמו Boston Scientific. הירשמו עכשיו ומצאו את עבודת החלומות שלך עם אקספוינט!
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United States
State
Marlborough
30 jobs found
04.09.2025
BS

Boston Scientific Data Analytics Specialist - Finance Automation & United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
Maintain and troubleshoot Alteryx workflows that extract and transform data from SAP S4/HANA to support reporting and analytics. Support Tableau dashboard enhancements and performance optimizations. Identify and resolve data quality...
Description:


Key Responsibilities:

  • Maintain and troubleshoot Alteryx workflows that extract and transform data from SAP S4/HANA to support reporting and analytics.
  • Support Tableau dashboard enhancements and performance optimizations.
  • Identify and resolve data quality or integration issues across the pipeline.
  • Collaborate cross-functionally with Finance, Accounting, Tax, and IT teams to ensure reporting accuracy and relevance.
  • Assist in implementing new business requirements, testing enhancements, and deploying updates.
  • Document workflows and maintain knowledge artifacts for ongoing support and auditability.
  • Analyze changes in SAP S4 data models and recommend adjustments to data pipelines.
  • Execute solution and monitor solution performance; proactively flag issues or risks to data integrity.
  • Participates in periodic audits and analyses to ensure accuracy, optimization of systems and reporting

Required Qualifications:

  • Bachelor’s degree in Information Systems, Computer Science, Business Analytics, Accounting, Finance, or a related field.
  • 2+ years of experience with data analytics tools, especially Alteryx and Tableau.
  • Working knowledge of SQL and SAP HANA data extraction.
  • Basic familiarity with accounting, finance, or tax data flows and concepts.
  • Strong problem-solving and communication skills, exceptional attention to detail

Preferred Qualifications:

  • Experience with SAP S4/HANA.
  • Tableau or Alteryx certification.
  • SQL
  • Prior experience supporting data pipelines in a financial or supply chain context.
  • Exposure to continuous monitoring or audit analytics.

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.

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04.09.2025
BS

Boston Scientific Field Sales Business Analyst II Urology United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
Provide effective support for the local team by responding to all requests in a timely, accurate and efficient manner. Provide Ad-hoc analytical support to the Local Region Manager teams as...
Description:

Your responsibilities will include:

  • Provide effective support for the local team by responding to all requests in a timely, accurate and efficient manner.
  • Provide Ad-hoc analytical support to the Local Region Manager teams as needed.
  • Utilize available reporting tools and technology to deliver intuitive analyses to the field.
  • Act as a process expert and liaison for the Sales team to internal departments.
  • Identify opportunities within the division by monitoring trends, performance metrics and relevant external data.
  • Produce customized business reviews that incorporate market conditions and challenges unique to the region and customer.
  • Provide local support and individual training for corporate initiatives and enablers such as Tableau, Sales Force and Windows 10.
  • Support Region/Divisional meeting preparation and execution.
  • Participate in strategic projects as required.
  • Support key initiatives like Quarterly Business Reviews and GPO Contract launches by working closely with RMs.
  • Work on key internal Sales Operations and Corporate projects as necessary.

What we're looking for in you:

  • Bachelor’s Degree
  • Minimum of 2 years of experience in a sales or financial analyst.
  • Proven analytical and problem-solving experience.
  • Strong back office application skills, including expert level Excel and some exposure to MS Access, Salesforce, SQL and some programming languages.
  • Demonstrated ability to balance multiple priorities against strict deadlines while maintaining a high degree of accuracy, attention to detail, and customer service.
  • Travel 10% of the time required.

Preferred Qualifications:

  • Excellent interpersonal skills and above average writing and verbal communication skills working with individuals at all levels of the organization.
  • Organization skills and the ability to handle work of a highly confidential nature.
  • Desire to work in a collaborative, teamwork-oriented environment.
  • 2+ years of experience within medical device industry.
  • At least 2 years supporting field sales organization.

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.

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03.09.2025
BS

Boston Scientific Medical Affairs Specialist III United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
Develop and implement global evidence generation strategies to support business objectives, product value and effectiveness. Lead cross-functional teams in designing and executing evidence generation plans. Stay abreast of current and...
Description:

Your responsibilities will include:

  • Develop and implement global evidence generation strategies to support business objectives, product value and effectiveness.

  • Lead cross-functional teams in designing and executing evidence generation plans.

  • Stay abreast of current and innovative analytical methodologies, tools, and applications to ensure state-of-the art evidence generation architecture, platforms, data, and analyses.

  • Collaborate with stakeholders to align and integrate evidence generation activities with overall business objectives.

  • Continuously assess and analyze operations and processes to identify opportunities for alignment, optimization and efficiency improvements related to EGS.

  • Design and deploy tailored tools and frameworks to enable stakeholders to consistently and effectively implement evidence strategies.

  • Implement strategies to identify and eliminate duplicative processes and efforts related to EGS across divisions, regions, and functional areas.

  • Stay current with applicable regulations, industry trends, and best practices in evidence generation to ensure compliance.

Required qualifications:

  • Minimum Bachelor's degree in health science or a related discipline.

  • Minimum 3 years of professional experience in evidence planning, clinical research, or related fields.

  • Proven understanding of medical device total product lifecycle, clinical studies and utility of alternative evidence generation activities.

  • Proven track record of leading and managing global evidence generation projects.

Preferred qualifications:

  • Advanced degree Master’s or a Ph.d in a relevant field (e.g., life sciences, public health, health economics, epidemiology)

  • Previous experience in medical device industry preferred

  • Proven experience in creating evidence strategies within rapidly changing organizational environments

  • Proven ability to build relationships, lead, and educate with excellent interpersonal and influence management skills

  • Preferred Applied Market Analytics knowledge.

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.

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03.09.2025
BS

Boston Scientific Sr Clinical QA Specialist United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
Participates in clinical project teams, and always influences clinical teams toward a state of inspection readiness. Plans, schedules, and conducts internal and external quality assurance audits of the systems, clinical...
Description:

Spencer Gregory Hale

Your responsibilities will include:

  • Participates in clinical project teams, and always influences clinical teams toward a state of inspection readiness

  • Plans, schedules, and conducts internal and external quality assurance audits of the systems, clinical investigative site audits, procedures, and controls employed in the design, conduct, and analysis of clinical trials

  • Assesses sponsor/investigator/monitor compliance with protocol, GCP and applicable regulatory requirements and relevant BSC policies and procedures

  • Assesses the accuracy, validity, and quality of the scientific data generated during clinical trials

  • Participates in problem-solving with clinical project teams at investigator sites

  • Communicate observations to clinical investigators and clinical program managers

  • Documents audit observations; evaluates impact and responses to audit findings and ensures the appropriate corrective actions are completed

  • Ensures tracking of audit findings

  • Contributes to the development of audit procedures and processes

  • Assists clinical QA Managers with annual audit planning, review and trending of audit results, and development and implementation of improvement initiatives

  • Assists in the preparation of investigator sites for FDA or other regulatory agency inspections and assists in preparation of written responses to findings

  • Keeps abreast of and interprets current worldwide regulatory requirements; advises management on the possible ramifications of regulatory changes

  • Support the Clinical organization in meeting BSC Quality system requirements

  • Supports the CAPA process, working cooperatively with Clinical NCEP/CAPA owners and providing quality input

  • Partner with Clinical to support supplier and BSC-related nonconformances by performing the following activities (NCEP, CAPA, SCARS):

  • Conduct root cause analysis

  • Determine corrective and preventive actions

  • Determine verification of effectiveness actions to support the corrective and preventive actions

  • Support IC CQA portfolio activities and quality system deliverables for IC CQA, including but not limited to quarterly audit schedule updates, management of IC CQA surveillance activities, communication of quality signals to quality leads and clinical leadership, and coordination of clinical and clinical quality QMR deliverables for ICTx and WM.

  • Proactively drive clinical compliance, making data-driven decisions to facilitate process improvement and a proactive quality culture.

  • Participates in the development, implementation, and maintenance of global quality systems. Works to identify ways to improve compliance with regulations and BSC policies and procedures for CQA

Quality System Requirements:

  • In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance with the Quality Policy and all other documented quality processes and procedures.

  • Assures that appropriate resources (personnel, tools, etc.) are maintained to assure Quality System compliance and adherence to the BSC Quality Policy.

  • Establishes and promotes a work environment that supports the Quality Policy and Quality System.

  • Apply sound, systematic problem-solving methodologies in identifying, prioritizing, communicating, and resolving quality issues.

What we're looking for in you:

Required Qualifications:

  • Bachelor’s degree in science, health, engineering or a relevant field of expertise

  • 5-7 years of work experience with quality systems/controlled processes

  • Previous experience in medical device or pharmaceutical industry in an area regulated by GCP regulations and guidelines

  • Strong presentation, communication, and critical thinking skills

  • Strong understanding of Quality Systems

  • Working knowledge of ISO 14155 and GCP

  • Working knowledge of ISO 13485

  • NCEP, CAPA, and Supplier Corrective Action experience

Preferred qualifications:

  • Working knowledge of US and International regulations and standards applicable to BSC

  • Additional quality certifications from ASQ, SOCRA, RQAP-GCP, etc.

  • Experience working cross-functionally with multiple stakeholders

  • NCEP, CAPA, and Supplier Corrective Action experience

  • Ability to collaborate and influence across multiple, cross-functional teams

Maximum Salary: $ 164500

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.

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.

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03.09.2025
BS

Boston Scientific Regulatory Affairs Specialist III United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
May work with R&D leadership to define technical roadmaps aligned with business objectives. Drive continuous improvement in engineering processes and methodologies. Collaborate with Regulatory Affairs, Clinical, Quality and Manufacturing teams...
Description:

About the role:

Boston Scientific is looking for a Senior Principal/Fellow Electrical Engineer. You will be responsible for providing electrical and electronic engineering support and expertise in the definition, design, development and test of products in accordance with the Quality system standards, Design Controls and customer requirements. Ensures products are designed to facilitate manufacturability.

Your responsibilities will include:

  • May work with R&D leadership to define technical roadmaps aligned with business objectives.
  • Drive continuous improvement in engineering processes and methodologies.
  • Collaborate with Regulatory Affairs, Clinical, Quality and Manufacturing teams etc. throughout product lifecycle.
  • Participate in executive reviews and strategic planning sessions.
  • Maintains substantial knowledge of state-of-the-art principles and theories in their particular area of expertise.
  • Provides critical design and technical problem resolution.
  • Assume technical lead in the design, development, and testing of complex bioelectronic systems comprised of PCB design, stimulation, power management, wireless communication, and sensing technologies, etc.
  • May lead projects or project teams with moderate resource requirements, risk, and/or complexity.
  • Can work independently within functional / divisional policies while maintaining good communication with functional and cross-functional teams.
  • May help with technical recruitment, training, and ongoing support of staff.
  • Provides technical guidance, training and mentorship to less senior staff contributing to their ongoing development within the company.
  • Provides feedback to the development staff on customer specific enhancements as well as new applications for base product in accordance with Quality System requirements.
  • Ensures new products or product enhancements are designed to facilitate transfer to manufacturing in a timely fashion and in accordance with Quality System requirements. Facilitates the process of transferring products from development to manufacturing.
  • Ensures that engineering testing and documentation is in accordance with regulatory requirements for approval of products by the regulatory agencies of the countries into which the products will be marketed.
  • Works with patent attorneys in documenting innovative ideas, reviewing patent application, and supporting Freedom to Operate Analysis.
  • Converts complex information to compelling business context and advice.
  • Presents convincing arguments for complex ideas and projects at cross-functional meetings in a way that persuades others to agree on recommendation and/or approach, when appropriate.

Required qualification:

  • Bachelor’s degree in engineering or related discipline or equivalent experience. Master’s degree or higher in engineering is preferred.
  • 10+ years’ experience in medical device design or similar products.
  • Experience working under and knowledge of quality systems designed to meet FDA/EU regulatory requirements.
  • Experience and knowledge of pre-clinical testing of medical products.
  • Ability to travel 20% of the time.

Preferred qualifications:

  • Demonstrates strong proficiency in Electrical Engineering, especially in analog circuit design.
  • Ability to adapt and learn quickly leveraging knowledge towards the contribution of projects.
  • Ability to use Microsoft Office tools for documentation, analyzing data, presenting data or ideas, etc.
  • Ability to use Microsoft Excel and other data analysis tools to manipulate and analyze data sets.
  • Competence in the use of Electronics CAD software (Altium) for schematic capture and PCB layout is preferred.
  • Professional, clear verbal and written communications skills required.
  • Ability to work independently or in a team setting as required.

Maximum Salary: $ 243000

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.

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26.07.2025
BS

Boston Scientific Principal Field Clinical Engineer - Northeast United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
The Principal Field Clinical Engineer (FCE) supports a growing department that manages a large pivotal study program based on an innovative medical device technology platform. The Senior FCE will be...
Description:


The Principal Field Clinical Engineer (FCE) supports a growing department that manages a large pivotal study program based on an innovative medical device technology platform. The Senior FCE will be responsible for all aspects of case support and product education aimed at treating product education involving coronary interventions, including calcium modification. This role will be reporting to Director, Field Clinical Operations.





⦁ Minimum Bachelor’s degree in Engineering, Anatomy, Physiology related field or equivalent healthcare experience required.
⦁ Minimum 5 years of experience in clinical research experience including coordinating multi-center trials with established technical expertise and knowledge
⦁ Ability to travel upto 75-90% domestically and internationally. Visits include clinical sites and centers.
⦁ Experience in presenting, writing and teaching clinical and medical information
⦁ Experience with group presentations and hands-on experience with surgical catheter based interventions
⦁ Must be able to work effectively with internal groups such as R&D, Quality, Regulatory, technical specialists, and external stakeholders achieve assigned goals
⦁ Ensure compliance with clinical study protocol, and identifying areas of concern and escalating when appropriate


⦁ Excellent written and verbal communication skills, very strong interpersonal skills including proficiency in medical terminology
⦁ Clinical Research experience in Medical Device
⦁ Experience coordinating multi-center Cardiology trials
⦁ Knowledge of Good Clinical Practices and trials, including feasibility IDE and post- market studies.

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.

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18.07.2025
BS

Boston Scientific EH & Specialist United States, Massachusetts, Marlborough

Limitless High-tech career opportunities - Expoint
Providing EHS site support for internal customers including training environments, commercial office environments, process development, and research and development laboratories. Identifying opportunities to minimize risks and prevent workplace injuries; work...
Description:

About the Role:

As an advocate for environment, health, and safety as core values at Boston Scientific, the EHS Specialist assists in the development and support of programs, policies, and procedures to ensure compliance with company requirements and all regulations pertaining to the site. The incumbent will provide guidance, training, and support, while influencing engagement and contributions from EHS colleagues, internal stakeholders, and external resources to drive continuous improvement initiatives.

Your responsibilities will include:

  • Providing EHS site support for internal customers including training environments, commercial office environments, process development, and research and development laboratories
  • Identifying opportunities to minimize risks and prevent workplace injuries; work with cross-functional teams to drive projects and support continuous improvement initiatives
  • Administrating ISO45001 Health & Safety Management System including internal/external audit facilitation and risk management; identify opportunities for improvement, implement recommendations and manage related documentation
  • Assisting with accident/incident investigations, root cause analysis and after-action reviews; collaborate with process owners to develop and implement corrective actions and engineering controls as needed
  • Coordinating with intercompany resources who work with regulatory agencies to conduct site inspections; provide guidance and safety recommendations for processes, equipment, and facility infrastructure design
  • Assisting with risk assessments on processes, equipment, and chemicals; identify compliance concerns, program non-conformities and opportunities for improvement
  • Assisting with EHS audits, self-assessments, and inspections to ensure workplace conditions comply with internal policies, program requirements and applicable local, state, and national regulations
  • Fostering relationships with contracted safety services and consultants
  • Supporting EHS-related committees, task forces, and cross-functional teams; serve on site emergency response team(s)
  • Supporting regulatory compliance activities including coordinating work efforts and recordkeeping related to chemical exposure monitoring (industrial hygiene), confined spaces, electrical safety, emergency action planning, equipment safety (machine guarding), fire prevention, chemical hygiene / lab safety, laser safety, contractor safety, respiratory protection, and safe facility design

Required qualifications:

  • Bachelor’s degree in occupational safety, safety engineering, safety management, occupational health, or similar discipline
  • Minimum 1 year of EHS experience in a commercial office, laboratory, industrial or manufacturing environment
  • Minimum 1 year of experience with safety-related programs, policies, procedures and regulations

Preferred qualifications:

  • Experience working in pharmaceutical, medical device, electronics, or similarly regulated industry
  • Experience with ergonomic risk reduction, emergency response and incident command in a manufacturing, laboratory, or office setting
  • Associate Safety Professional (ASP), Hazardous Waste Operations and Emergency Response (HAZWOPER)
  • Strong interpersonal skills and ability to lead and influence cross-functional teams

Maximum Salary: $ 115900

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.

Show more

These jobs might be a good fit

Limitless High-tech career opportunities - Expoint
Maintain and troubleshoot Alteryx workflows that extract and transform data from SAP S4/HANA to support reporting and analytics. Support Tableau dashboard enhancements and performance optimizations. Identify and resolve data quality...
Description:


Key Responsibilities:

  • Maintain and troubleshoot Alteryx workflows that extract and transform data from SAP S4/HANA to support reporting and analytics.
  • Support Tableau dashboard enhancements and performance optimizations.
  • Identify and resolve data quality or integration issues across the pipeline.
  • Collaborate cross-functionally with Finance, Accounting, Tax, and IT teams to ensure reporting accuracy and relevance.
  • Assist in implementing new business requirements, testing enhancements, and deploying updates.
  • Document workflows and maintain knowledge artifacts for ongoing support and auditability.
  • Analyze changes in SAP S4 data models and recommend adjustments to data pipelines.
  • Execute solution and monitor solution performance; proactively flag issues or risks to data integrity.
  • Participates in periodic audits and analyses to ensure accuracy, optimization of systems and reporting

Required Qualifications:

  • Bachelor’s degree in Information Systems, Computer Science, Business Analytics, Accounting, Finance, or a related field.
  • 2+ years of experience with data analytics tools, especially Alteryx and Tableau.
  • Working knowledge of SQL and SAP HANA data extraction.
  • Basic familiarity with accounting, finance, or tax data flows and concepts.
  • Strong problem-solving and communication skills, exceptional attention to detail

Preferred Qualifications:

  • Experience with SAP S4/HANA.
  • Tableau or Alteryx certification.
  • SQL
  • Prior experience supporting data pipelines in a financial or supply chain context.
  • Exposure to continuous monitoring or audit analytics.

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.

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בואו למצוא את עבודת החלומות שלכם בהייטק עם אקספוינט. באמצעות הפלטפורמה שלנו תוכל לחפש בקלות הזדמנויות Field Managed Care Specialist בחברת Boston Scientific ב-United States, Marlborough. בין אם אתם מחפשים אתגר חדש ובין אם אתם רוצים לעבוד עם ארגון ספציפי בתפקיד מסוים, Expoint מקלה על מציאת התאמת העבודה המושלמת עבורכם. התחברו לחברות מובילות באזור שלכם עוד היום וקדמו את קריירת ההייטק שלכם! הירשמו היום ועשו את הצעד הבא במסע הקריירה שלכם בעזרת אקספוינט.