Arden Hills, MN, US
5 days ago
Senior R&D Manager - Electrophysiology

Additional Location(s):  N/A

Diversity - Innovation - Caring - Global Collaboration - Winning Spirit - High Performance

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.                

 

At Boston Scientific, we’ll give you the opportunity to harness all that’s within you by working in teams of diverse and high-performing employees, tackling some of the most important health industry challenges. With access to the latest tools, information and training, we’ll help you in advancing your skills and career. Here, you’ll be supported in progressing – whatever your ambitions.  

 

Electrophysiology is an exciting growth driver for BSC. With the acquisition of FARAPULSE Inc., Boston Scientific has strengthened its leadership in Personalized EP Solutions, with a strong focus in Atrial Fibrillation. You will oversee the development and management of staff resources in the creation and development of new, robust, high-quality, manufacturable electrophysiology ablation catheter technologies. 

 

About the role: 

As Senior R&D Manager you will be a key member of the EP Therapy Systems Product Development team. Your primary responsibility will be leading a team of R&D engineers in driving the advancement of new products and technologies for the Electrophysiology division. The successful candidate will manage and provide technical guidance to an interdisciplinary team of professionals in support of the development of electronic medical systems. 

 

This position is for a hands-on technical leader responsible for directing the activities of the systems engineering group focused on new product development. As Senior R&D Manager, you will lead and be a part of a high-performance team responsible for the design, implementation, and test of electronic medical systems and their associated devices within our electrophysiology pulsed field ablation portfolio. This critical role will lead best-in-class development practices and rigorous, holistic product design in coordination with internal and external partners. The ideal candidate will exhibit a blend of technical knowledge, business acumen, coaching ability, fact-based decision making, project management expertise, and collaborative stakeholder management. In return for your unique combination of big-picture perspective, ability to inspire and develop a high-performing team, and strong desire to win in the marketplace, you'll be a trusted leader collaborating with some of most dynamic minds in the business. You will foster an environment that encourages people to take measured risks, learn from mistakes, and push the boundaries of engineering.  

 

Key Responsibilities: 

Lead teams in the achievement of organizational and functional goals.  Guide, coach, direct, and develop direct reports, and if applicable, drive those practices throughout their organization. 

Recruit, coach, and develop organizational talent. 

Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. 

Collaborate with senior technical leaders, project management, and inter-disciplinary partners 

Coach and lead engineering teams to develop technical aspects of complex single use device development including requirements, design, implementation, test, integration, transfer to manufacturing, and verification/validation. Establish meaningful goals that define success. 

Develop detailed work plans, budgets, objectives, schedules, project estimates, resource plans, and status reports. Monitor and troubleshoot performance and schedule issues. Support and enable team to achieve objectives. 

Foster a diverse workplace that enables all participants to contribute to their full potential in pursuit of organizational objectives. 

Keep the organization's vision and values at the forefront of decision making and action. 

Build strategic partnerships and effectively collaborate cross-functionally to further departmental and organizational objectives. 

Understand the external requirements that govern product development and the notified body approval processes for various phases of product evaluation (i.e., FIH, IDE, commercial). Ensure quality system compliance for medical device development, champion continuous improvement, and adopt best practices.  

Strong hands-on capabilities to act as the system architect and integration lead to drive technical decision-making with a deep understanding of electromechanical systems. 

Develop solutions to diverse engineering problems of high complexity which require the regular use of ingenuity and creativity. Leverage internal/external partners as necessary to achieve project objectives. 

Work across multiple design/product workstreams in a capacity to resolve complex problems with robust technical solutions. Consider all critical aspects of product design during decision making including patient safety, clinical practice, high-level product performance, and product manufacturability. 

Solve system problems by analyzing the situation and recommending corrective or alternative actions. Lead technical teams through problem solving. Facilitate crisp decision making around key technical issues. 

Lead by example and motivate and inspire other technical team members in the program. 

Create a strong team culture around high expectations and high performance. 

Demonstrate effective change leadership. 

Provide clear communication to stakeholders at key technical updates. 

 

Required qualifications: 

BS degree in Mechanical Engineering  

Required minimum years of work experience (primarily in medical device or related field): 7+ years with BS, 5+ years with MS 

5+ years’ experience in leading and developing a medical device technical engineering group  

Proficient in design controls and risk management practices with fluency in what external regulations require for various product approvals 

Highly creative problem solver who leads with a sense of urgency 

Demonstrated strong cross-functional collaboration, influence without authority, and project/task  management enabling highly effective teams   

Passion for understanding and solving problems for end users  

Passion for understanding the end user environment with a fluency in design validation and usability to confirm design solutions 

A proven track record developing medical devices from early stage through full product launch and sustaining 

Personal drive, individual accountability and a strong bias for action 

Strong personal credibility and excellent communication skills 

Preferred qualifications: 

Experience in electrophysiology, cardiac rhythm management, structural heart or a comparable intracardiac technology 

Fluency in the IEC 60601 standards 

 

 

 

Requisition ID: 589960


As a leader in medical science for more than 40 years, we are committed to solving the challenges that matter most – united by a deep caring for human life. Our mission to advance science for life is about transforming lives through innovative medical solutions that improve patient lives, create value for our customers, and support our employees and the communities in which we operate. Now more than ever, we have a responsibility to apply those values to everything we do – as a global business and as a global corporate citizen.

 

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!

 

At Boston Scientific, we recognize that nurturing a diverse and inclusive workplace helps us be more innovative and it is important in our work of advancing science for life and improving patient health. That is why we stand for inclusion, equality, and opportunity for all. By embracing the richness of our unique backgrounds and perspectives, we create a better, more rewarding place for our employees to work and reflect the patients, customers, and communities we serve. 

 

 

Boston Scientific Corporation has been and will continue to be an equal opportunity employer. To ensure full implementation of its equal employment policy, the Company will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identify, gender expression, veteran’s status, age, mental or physical disability, genetic information or any other protected class.

 

 

Boston Scientific maintains a prohibited substance free workplace. Pursuant to Va. Code § 2.2-4312 (2000), Boston Scientific is providing notification that the unlawful manufacture, sale, distribution, dispensation, possession, or use of a controlled substance or marijuana is prohibited in the workplace and that violations will result in disciplinary action up to and including termination.

 

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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