דרושים מנהל פרוייקט ב-Boston Scientific ב-United States, Waltham

About the role:

The person in this role will be a leader of projects and programs within the EP Project Management group, specifically for the Opal HDx Mapping System. The scope of projects may include activities from initial product development to the end of product life cycle across business units and manufacturing sites. Success in the role requires a focus on capturing the opportunities from across the various functions, creating a cohesive strategy for project execution and driving execution to ensure project completion.

Project size will range from small one-off tasks to large process improvement, design change, line extension activities, design transfers and projects driving global productivity and commercialization. Multiple projects will be handled simultaneously with cross-functional team members from R&D, Design Assurance, Packaging, Regulatory, Operations, Supplier Development, Supply Chain and Clinical. Strong interpersonal and communication skills as well as the ability to build relationships are required for this role.

Your responsibilities include:

• Developing, executing and leading of project/program teams to successfully deliver the defined products/solutions to business unit management (initiating, planning, executing, controlling, and closing processes)
• Identifying resources required for assigned project activities and forming teams to complete the activities
• Building team ownership and commitment to project plan
• Developing and monitoring project budgets through regular analysis of cost and spending
• Timely communication of priorities and status with senior management, regional and functional leads including presentations and discussions at FLT (Franchise Leadership Team) and PIB (Product Investment Board)
• Managing challenges of technology application and new product development including identification, communication and escalation of technical and business risks
• Resolving conflicts with team members and providing input to functional managers on team and team member performance
• Facilitating end of life of products following commercial release of new products
• Mentoring and/or coaching other functional and project managers
• Fostering a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives
• Monitoring and ensuring compliance with company policies and procedures (e.g. federal/country and regulatory requirements)
• Managing changing business priorities, while keeping the team focused
• Setting clear expectations for both the project team as well as management in terms of delivery as it pertains to prioritization, scope, time, and resources

Required qualifications:

• Bachelor’s degree
• 5+ years of related work experience or equivalent combination of education and work experience; new product development ideal
• Strong organization, communication and influencing skills, as well as a demonstrated ability to confidently handle full responsibility for project completion
• Results-oriented and focused on delivering timely, accurate and premium execution
• Experience in managing multiple significant, cross functional projects and/or initiatives

Preferred qualifications and competencies:

• BS Degree, Engineering
• PMP Certification
• Background in medical device development
• Knowledge of DHF, DMR and Engineering Change processes
• Experience communicating and influencing all levels of the organization
• Experience managing sustaining and new product development projects including business critical and high visibility projects
• Demonstrated ability to lead small and medium cross functional teams as a Project Manager, Operations Leader or Technical Leader
• Product knowledge of EP products and processes

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.

Electrophysiology R&D Engineering Intern

We will consider qualified applicants of all ages who are starting (or restarting) their careers

Our Purpose:

As a R&D Engineering Intern at Boston Scientific, you will…

• Use your problem-solving abilities to perform meaningful engineering work.

• Have opportunities to expand your professional network.

• Grow your skillset through a combination of training, hands-on experience, and mentorship.

• Collaborate with a cross-functional team.

• Get exposure to what it is like working in a Fortune 500 medical device company.

• Design, fabricate, and test prototype devices to address clinical feedback.

• Analyze large clinical databases to inform device design and procedural technique.

• View live and recorded clinical procedures and developing test methods to replicate use.

Required Qualifications:

• Must graduate between Fall 2026 and Spring 2027

• Currently pursuing a degree in Mechanical or Biomedical Engineering (or emphasis/minor in either)
• Must be able to commit to one of the following full internship program periods: May 18th – August 7th OR May 26th – August 14th
• Must be eligible to work in the U.S. without company sponsorship, now or in the future, for employment-based work authorization

• Must have reliable transportation to and from the Arden Hills, MN Boston Scientific Corporate location

• Must have knowledge of analytical techniques and statistical analysis.

Preferred Qualifications:

• Ability to communicate effectively with diverse, cross-functional teams.

• Passion to learn new technologies and find new solutions.

Maximum Salary: $ 97,760

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.

Purpose Statement:

The Systems Engineering Manager will provide leadership, vision, and direction within the EP systems engineering organization. In the role of Manager, you will be responsible for supporting the growth and continued development of the Systems Engineering team and function; overseeing technical staff members and helping to define and foster functional excellence. You will have the opportunity to significantly impact the development of truly life changing patient therapies for the relief of debilitating diseases.

Responsibilities:

• Lead a team of system engineers including recruiting, hiring, mentoring, professional development, and performance coaching.
• Develop the system engineering discipline cross functionally through focus on system architecture, interfaces, and a system of systems mindset.
• Oversee and drive the system of system development lifecycle, from design and development to testing, deployment, maintenance, and security.
• Oversee systems requirements development and requirements management tool development.
• Support planning and execution of systems level testing, including manual and automated systems test development.
• Support organizational competency in translating clinical needs to NPD teams.
• Responsible for organizational fluency in key standards for capital equipment and SUD such as ISO 60601.
• Support a high-performing team culture and entrepreneurial environment where people are highly engaged, skilled, and collaborative.
• Help build engagement within the site and team.
• Effectively communicate with different levels of management, as well as business and technical employees.
• Demonstrate effective change leadership.
• Demonstrate ability to succeed in fast paced environment while managing multiple projects simultaneously.
• Deep dive technically where needed while keeping a broad perspective.
• Build strong collaboration with development sites and cross-functional partners.
• Cultivate a culture of continuous improvement by staying informed about industry trends, technological advancements, and emerging tools in medical device systems engineering, human factors, design controls, and testing.
• Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
• Keeps the organization's vision and values at the forefront of decision making and action.
• Monitor and ensure compliance with company policies and procedures.
• Travel expectations 25-30%

Requirements:

• Successful history of launching and maintaining products within the medical device industry
• Demonstrated expertise in systems engineering for the design, development and testing of medical devices.
• Demonstrate a keen interest in EP, workflows, clinical features, and user experience.
• Ability to lead a cross functional site and build engagement.
• Ability to lead a multi-site team and collaborate with peers in different locations.
• Experience working with requirement management, collaboration, and issue tracking tools such as Jama and Jira.
• Working knowledge of hardware, firmware, and software evaluation to standards such as IEC 62304 and ISO 60601
• Lead a group or team of employees in the development and achievement of organizational goals. Guide, coach, direct, and develop direct reports, and if applicable, drive those practices throughout their organization.
• Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
• Ability to direct and control the activities, budget, and headcount for the systems engineering organization.
• Monitor and ensure compliance with company policies and procedures (e.g. federal/country and regulatory requirements).
• Bachelor of Science degree in a relevant engineering discipline with 10+ years of experience developing highly complex systems
• 5+ years’ experience managing technical teams in the development of medical device system of systems

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.

Purpose Statement:

The Systems Engineering Senior Manager will provide leadership, vision, and direction within the EP systems engineering organization. In the role of Senior Manager, you will be responsible for supporting the growth and continued development of the Systems Engineering team and function; overseeing technical staff members and helping to define and foster functional excellence. You will have the opportunity to significantly impact the development of truly life changing patient therapies for the relief of debilitating diseases.

Responsibilities:

• Lead a team of system engineers including recruiting, hiring, mentoring, professional development, and performance coaching.
• Develop the system engineering discipline cross functionally through focus on system architecture, interfaces, and a system of systems mindset.
• Oversee and drive the system of system development lifecycle, from design and development to testing, deployment, maintenance, and security.
• Oversee systems requirements development and requirements management tool development.
• Support planning and execution of systems level testing, including manual and automated systems test development.
• Support organizational competency in translating clinical needs to NPD teams.
• Responsible for organizational fluency in key standards for capital equipment and SUD such as ISO 60601.
• Support a high-performing team culture and entrepreneurial environment where people are highly engaged, skilled, and collaborative.
• Help build engagement within the site and team.
• Effectively communicate with different levels of management, as well as business and technical employees.
• Demonstrate effective change leadership.
• Demonstrate ability to succeed in fast paced environment while managing multiple projects simultaneously.
• Deep dive technically where needed while keeping a broad perspective.
• Build strong collaboration with development sites and cross-functional partners.
• Cultivate a culture of continuous improvement by staying informed about industry trends, technological advancements, and emerging tools in medical device systems engineering, human factors, design controls, and testing.
• Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
• Keeps the organization's vision and values at the forefront of decision making and action.
• Monitor and ensure compliance with company policies and procedures.
• Travel expectations 25-30%

Requirements:

• Successful history of launching and maintaining products within the medical device industry
• Demonstrated expertise in systems engineering for the design, development and testing of medical devices.
• Demonstrate a keen interest in EP, workflows, clinical features, and user experience.
• Ability to lead a cross functional site and build engagement.
• Ability to lead a multi-site team and collaborate with peers in different locations.
• Experience working with requirement management, collaboration, and issue tracking tools such as Jama and Jira.
• Working knowledge of hardware, firmware, and software evaluation to standards such as IEC 62304 and ISO 60601
• Lead a group or team of employees in the development and achievement of organizational goals. Guide, coach, direct, and develop direct reports, and if applicable, drive those practices throughout their organization.
• Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives.
• Ability to direct and control the activities, budget, and headcount for the systems engineering organization.
• Monitor and ensure compliance with company policies and procedures (e.g. federal/country and regulatory requirements).
• Bachelor of Science degree in a relevant engineering discipline with 10+ years of experience developing highly complex systems
• 8+ years’ experience managing technical teams in the development of medical device system of systems.

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.

Your responsibilities will include:

• Determines clear and specific priorities for the development of new cardiac mapping software and software enhancements for pulsed field ablation by defining user needs and working with other internal functional groups.
• Leads voice-of-customer (VOC) and voice-of-business (VOB) activities for current and proposed investments. Formulates recommendations based on data collected and advocates for customer needs while collaborating on product inputs and clinical benchmarks.
• Constructively gathers input and challenges assumptions with Global counterparts to refine product decisions. Makes recommendations on product launch cadence leveraging a broad organizational, technical capability and competitive perspective.
• Positively represents the company by visiting accounts and users to solicit feedback on company products and services.
• Consolidates and disseminates a deep understanding of the competitive global EP landscape. Contribute to understanding key industry dynamics in formulating technology, clinical and commercial strategies. Supports regional training of marketing and sales teams.
• Develop and leverage marketing insights to define marketing claims and value propositions.
• Network with colleagues in other divisions and cross-functional departments to align strategies and opportunities.
• Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all regulations governing the quality systems.

Required Qualifications

• Bachelor’s degree in Business, Engineering, Science, Healthcare/Biomedical fields.
• 5+ years of professional experience in the medical device industry, especially cardiovascular or electrophysiology fields.
• Flexibility to travel up to 20% in support of tradeshows, internal meetings and customer programs as required.

Preferred Qualifications

• Clinical EP experience, including mapping specialist
• Advanced degrees, including M.S, PhD or MBA.
• Proven track record of Physician and KOL engagement.

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.

Your responsibilities will include:

• Determines clear and specific priorities for the development of new cardiac mapping software and software enhancements for pulsed field ablation by defining user needs and working with other internal functional groups.
• Leads voice-of-customer (VOC) and voice-of-business (VOB) activities for current and proposed investments. Formulates recommendations based on data collected and advocates for customer needs while collaborating on product inputs and clinical benchmarks.
• Constructively gathers input and challenges assumptions with Global counterparts to refine product decisions. Makes recommendations on product launch cadence leveraging a broad organizational, technical capability and competitive perspective.
• Positively represents the company by visiting accounts and users to solicit feedback on company products and services.
• Consolidates and disseminates a deep understanding of the competitive global EP landscape. Contribute to understanding key industry dynamics in formulating technology, clinical and commercial strategies. Supports regional training of marketing and sales teams.
• Develop and leverage marketing insights to define marketing claims and value propositions.
• Network with colleagues in other divisions and cross-functional departments to align strategies and opportunities.
• Demonstrate a primary commitment to patient safety and product quality. Understand and comply with all regulations governing the quality systems.

Required qualifications:

• Bachelor’s degree in Business, Engineering, Science, Healthcare/Biomedical fields.
• 5+ years of professional experience in the medical device industry, especially cardiovascular or electrophysiology fields.
• Ability to collaborate with and influence key stakeholders without direct authority.
• Flexibility to travel up to 20% in support of tradeshows, internal meetings and customer programs as required.
• Demonstrated ability to work independently and collaboratively to meet deadlines and manage all aspects of product development with a high degree of attention to detail.

Preferred qualifications:

• 3+ years in research, engineering or product development roles.
• Advanced degrees, including M.S, PhD or MBA.
• Experience with market and revenue modeling.
• Experience working globally across multiple countries/regions.
• Proven track record of Physician and KOL engagement.
• Excellent communication and interpersonal skills

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.