Principal Regulatory Affairs Specialist
Salary undisclosed
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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.
About the role:
At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. In the Urology division, we continually advance the quality of patient care with innovative urology solutions. We have a robust product line and pipeline, and we will continue to make an investment in Urology treatments. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. The role requires strong US, EU, China, and international regulatory experience that can be leveraged to help support international expansion.
This is a hybrid role (in office 3 days per week) based in Marlborough, MA.
Your responsibilities will include:
Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams
Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow-up of submissions under review
Assists with developing and implementing regulatory strategies for new and modified medical devices, as well as for OEM and Contract Manufacturer partnerships
Is a liaison for new business partners to provide regulatory guidance for US, EU, China, and international product registration
Acts as a core member on manufacturing and development teams, providing regulatory feedback and guidance throughout the product development cycle, and coordinating team inputs for submissions
Responsible for preparation and submission of global regulatory applications, as well as internal regulatory file documentation
Reviews device labeling and advertising materials for compliance with global regulations; analyzes and recommends appropriate changes
Reviews and signs-off on product and manufacturing changes for compliance with applicable regulations
Support and maintain Quality initiatives in accordance with BSC Quality Policy
Continuously assess ways to improve Quality
Develops and implements departmental and divisional policies and procedures
Supports highly technical or major business segment product lines, special projects or strategic initiatives
Required Qualifications:
A minimum of a Bachelor's Degree in a scientific, technical, or related discipline
A minimum of 8 years Regulatory Affairs experience in the medical industry
Prior experience of supporting both the capital equipment as well as single-use disposables
Prior experience with 510(k) submissions, EU MDR and international regulatory registrations
Working knowledge of FDA, EU and international regulations for medical devices
Ability to read and interpret global regulations and standards
General understanding of product development process, design control and quality system regulations
General understanding of regulations applicable to the conduct of clinical trials
Preferred Qualifications:
Prior experience supporting contract manufactured and/or OEM products
Ability to simultaneously manage several projects
Proficiency with Microsoft Office
Effective research and analytical skills
Effective written and oral communication, technical writing and editing skills
Ability to work independently with minimal supervision
#LI-Hybrid
Requisition ID: 593123
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.
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.
About the role:
At Boston Scientific, this is a place where you can find meaningful purpose, improving lives through your life's work. In the Urology division, we continually advance the quality of patient care with innovative urology solutions. We have a robust product line and pipeline, and we will continue to make an investment in Urology treatments. This role will be responsible for Regulatory Affairs support of submissions and ongoing regulatory compliance for product development process, as well as developing regulatory strategies and support for new business development efforts associated with external manufacturers (OEM) and contract manufacturers. The role requires strong US, EU, China, and international regulatory experience that can be leveraged to help support international expansion.
This is a hybrid role (in office 3 days per week) based in Marlborough, MA.
Your responsibilities will include:
Provides technical guidance and regulatory training/mentoring to other Regulatory Affairs employees and cross-functional teams
Acts as company representative, developing and maintaining positive relationships with device reviewers through oral and written communications regarding pre-submission strategy/regulatory pathway development, testing requirements, clarification and follow-up of submissions under review
Assists with developing and implementing regulatory strategies for new and modified medical devices, as well as for OEM and Contract Manufacturer partnerships
Is a liaison for new business partners to provide regulatory guidance for US, EU, China, and international product registration
Acts as a core member on manufacturing and development teams, providing regulatory feedback and guidance throughout the product development cycle, and coordinating team inputs for submissions
Responsible for preparation and submission of global regulatory applications, as well as internal regulatory file documentation
Reviews device labeling and advertising materials for compliance with global regulations; analyzes and recommends appropriate changes
Reviews and signs-off on product and manufacturing changes for compliance with applicable regulations
Support and maintain Quality initiatives in accordance with BSC Quality Policy
Continuously assess ways to improve Quality
Develops and implements departmental and divisional policies and procedures
Supports highly technical or major business segment product lines, special projects or strategic initiatives
Required Qualifications:
A minimum of a Bachelor's Degree in a scientific, technical, or related discipline
A minimum of 8 years Regulatory Affairs experience in the medical industry
Prior experience of supporting both the capital equipment as well as single-use disposables
Prior experience with 510(k) submissions, EU MDR and international regulatory registrations
Working knowledge of FDA, EU and international regulations for medical devices
Ability to read and interpret global regulations and standards
General understanding of product development process, design control and quality system regulations
General understanding of regulations applicable to the conduct of clinical trials
Preferred Qualifications:
Prior experience supporting contract manufactured and/or OEM products
Ability to simultaneously manage several projects
Proficiency with Microsoft Office
Effective research and analytical skills
Effective written and oral communication, technical writing and editing skills
Ability to work independently with minimal supervision
#LI-Hybrid
Requisition ID: 593123
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.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
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