Principal Regulatory Affairs Specialist
2 months ago
Additional Locations: 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.
Principal Regulatory Affairs Specialist – Endoscopy
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 Endoscopy division, we provide advance technologies for diagnosing and treating diseases of the digestive system, airway and lungs. We have a robust product line and pipeline, and we will continue to make an investment in Endoscopy treatments. This role in Regulatory Affairs will be responsible for 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.
Your responsibilities include:
-
Under minimal supervision, 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 team member on development teams, providing Regulatory Affairs feedback and guidance throughout the product development cycle.
-
Responsible for preparation and submission of regulatory applications, as well as internal regulatory file documentation.
-
Reviews device labeling and advertising materials for compliance with submissions and applicable 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.
What we're looking for in you:
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 with 510K submissions
-
Prior experience with Class III devices
-
Prior experience with EU MDR.
-
Prior experience with China and international regulatory requirements.
-
Working knowledge of FDA and international regulations for medical devices.
-
General understanding of product development process and design control.
-
General understanding of regulations applicable to the conduct of clinical trials.
Preferred qualifications:
-
Fluent in Mandarin
-
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.
Requisition ID: 588701
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
-
Regulatory Affairs Expert
3 weeks ago
Marlborough, Massachusetts, United States Boston Scientific Full timeTransforming Patient Care in UrologyAt Boston Scientific, we are dedicated to advancing the quality of patient care through innovative solutions. As a Principal Regulatory Affairs Specialist, you will play a crucial role in supporting our Urology division's mission to improve lives.Key Responsibilities:1. Collaborate with cross-functional teams to develop...
-
Regulatory Affairs Specialist
4 weeks ago
Marlborough, Massachusetts, United States IPG Photonics Full timeJob SummaryWe are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at IPG Photonics. As a key member of our regulatory team, you will be responsible for preparing and submitting global regulatory applications, reviewing device labeling and advertising materials, and maintaining regulatory files and tracking...
-
Senior Regulatory Affairs Specialist
4 weeks ago
Marlborough, Massachusetts, United States IPG Photonics Full time{"h1": "Regulatory Affairs Specialist at IPG Photonics", "p": "We are seeking a highly motivated and detail-oriented Regulatory Affairs Specialist to join our team at IPG Photonics. As a key member of our regulatory team, you will be responsible for preparing and submitting global regulatory applications, reviewing device labeling and advertising materials,...
-
Director of Regulatory Affairs
2 weeks ago
Marlborough, United States Hobson Prior Full timeHobson Prior is seeking a Director of Regulatory Affairs to join a leading biotechnology company. This position, based in the US (remote), will require working with a team located mainly in Europe and will therefore require both flexibility and the ability to work in an international environment. This role focuses on supporting new drug applications and...
-
Director of Regulatory Affairs
5 days ago
Marlborough, United States Hobson Prior Full timeHobson Prior is seeking a Director of Regulatory Affairs to join a leading biotechnology company. This position, based in the US (remote), will require working with a team located mainly in Europe and will therefore require both flexibility and the ability to work in an international environment. This role focuses on supporting new drug applications and...
-
Regulatory Affairs Expert
2 weeks ago
Marlborough, Massachusetts, United States Hobson Prior Full timeHobson Prior is a leading life sciences recruitment agency dedicated to connecting exceptional professionals with top biotechnology companies. As a Director of Regulatory Affairs, you will play a vital role in ensuring compliance with regulatory requirements and developing strategic plans for new drug applications.This position is based in the US and offers...
-
Clinical Evaluation Scientist II
7 days ago
Marlborough, Massachusetts, United States Boston Scientific Full timeWe are seeking a highly skilled Clinical Evaluation Scientist II to join our team in Global Regulatory Affairs. As a key member of our team, you will be responsible for ensuring the safety and efficacy of our products through systematic data analysis from multiple data sources.The ideal candidate will have a strong background in clinical evaluation,...
-
Principal System Engineer
7 days ago
Marlborough, United States Candela Full timePrincipal System Engineer Requisition Number 2782 Location US - Marlborough, MA State/Territory Massachusetts General Summary The Senior/Principal Systems Engineer will work across engineering functions to implement projects related to aesthetic laser systems and accessories. This person will work cross functionally (marketing, clinical, service,...
-
Principal Program Quality Lead
3 weeks ago
Marlborough, Massachusetts, United States RTX Full timeJob Title:Principal Program Quality LeadJob Summary:We are seeking a highly skilled Principal Program Quality Lead to join our team at Raytheon Technologies. As a key member of our quality assurance team, you will be responsible for promoting and executing a strong quality mindset, practices, knowledge sharing, and collaboration across our Naval Power...
-
Principal System Engineer
2 months ago
Marlborough, United States Candela Medical Full timeGeneral SummaryThe Senior/Principal Systems Engineer will work across engineering functions to implement projects related to aesthetic laser systems and accessories. This person will work cross functionally (marketing, clinical, service, manufacturing, regulatory, and quality organizations) to define, architect, and coordinate the implementation of...
-
Principal Financial Analyst
3 weeks ago
Marlborough, Massachusetts, United States Boston Scientific Full timeAbout the Role:The Finance team at Boston Scientific is seeking a highly skilled Principal Financial Analyst to join their Global HQ FinOps Process and Reporting team. This is an exciting opportunity to be part of a newly created finance team and help shape the future of the US FP&A organization. The new hub will facilitate standardized and streamlined...
-
Laboratory Specialist
4 weeks ago
Marlborough, Massachusetts, United States Metrowest Medical Center Full timeJob Summary: We are seeking a skilled Laboratory Specialist to join our team at Metrowest Medical Center. The ideal candidate will have a strong background in laboratory testing and a passion for delivering high-quality results. As a Laboratory Specialist, you will be responsible for processing and testing laboratory specimens, reviewing and reporting lab...
-
EHS Environmental Compliance Specialist
3 weeks ago
Marlborough, Massachusetts, United States MyHR Rescue Full timeAbout the job EHS Environmental SpecialistAt MyHR Rescue, we're seeking a highly motivated Environmental Specialist to join our team. As a key member of our Site Environmental, Health, and Safety (EH&S) Team, you'll be responsible for leading site environmental compliance, environmental improvement programs, and ensuring regulatory compliance.Key...
-
Senior Quality Assurance Specialist, CSV
4 weeks ago
Marlborough, Massachusetts, United States Moderna Full timeRole SummaryModerna is seeking a highly skilled Senior Quality Assurance Specialist, CSV to join our team. As a key member of our Quality Assurance department, you will be responsible for ensuring the compliance of computer system validation with regulatory requirements.Key Responsibilities:Review and audit computerized system validation deliverables...
-
RN Homecare Specialist
4 weeks ago
Marlborough, Massachusetts, United States Amedisys Full timeAbout AmedisysAmedisys is a leading provider of home health and hospice care services in the United States. Our mission is to deliver high-quality, patient-centered care that improves the lives of our patients and their families.Job SummaryWe are seeking a skilled and compassionate Registered Nurse (RN) to join our team as a Homecare Specialist. As a...
-
Business Process Administrative Specialist III
4 weeks ago
Marlborough, Massachusetts, United States Boston Scientific Full timeAbout the Role:Boston Scientific is seeking a highly skilled and detail-oriented individual to join our Global Business Services team as a Business Process Administrative Specialist III.In this role, you will be responsible for managing and entering critical data into SAP, our enterprise ERP system, ensuring all product certifications comply with regulatory...
-
Quality Assurance Specialist
4 weeks ago
Marlborough, Massachusetts, United States Integrated Resources Full timeJob SummaryWe are seeking a highly skilled Quality Assurance Specialist to join our team at Integrated Resources. The successful candidate will be responsible for ensuring the highest quality standards in our Post Market Quality department.Key ResponsibilitiesAssess complaints and assign the applicable complaint failure mode and determine if escalation is...
-
Clinical Trial Manager
3 weeks ago
Marlborough, Massachusetts, United States Boston Scientific Full timeAbout the Role:The Clinical Trial Manager will be responsible for the design, planning, execution, and leadership of clinical studies and clinical programs worldwide for Boston Scientific's Coronary Therapies portfolio.Responsible for leading cross-functional clinical teams in support of the organization's business objectives for product development and/or...
-
Marlborough, Massachusetts, United States Danaher Corporation Full timeWelcome to Danaher Corporation, a global leader in Life Sciences and Diagnostics. We are seeking a highly motivated Compliance Specialist to join our team in Marlborough, MA.Estimated salary: $60,000 - $80,000 per year, depending on experience.Job Summary:We are looking for a detail-oriented and business-focused Compliance Specialist to support our IT...
-
Pharmacovigilance Operations Specialist
4 weeks ago
Marlborough, Massachusetts, United States Sunrise Systems, Inc. Full timeJob Title: Pharmacovigilance Operations SpecialistJob ID: Location: Marlborough, MA Duration: 03 Months contract on W2 Responsibilities:The Pharmacovigilance Operations Specialist is responsible for the management of the Pharmacovigilance (PVRM) and non-PVRM vendor(s) (e.g. Commercial) and will be responsible for adverse event handling and reporting and for...