Work mode: Onsite
Onsite Location(s):

Yokneam, IL

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.

Responsible for Regulatory Affairs support of submissions and on going regulatory compliance for product development & changes support of both design and processes.

Main Duties:

Provide Regulatory read on product design and process changes to cross- functional teams
Act as a core member on manufacturing and remediation teams, providing regulatory feedback and guidance throughout the program, and coordinating team inputs for submissions
Complete Regulatory assessment forms and work with the international team on understanding the global implications of design and process changes
Coordinate submission activities including, but not limited to: US premarket approvals, international design dossiers, post-approval reports, export certificates, clinical trial exemptions and establishment registrations and listings
Work on the writing and review of documents to establish EU MDR Technical Documentation, also in preparation for submission to the Notified Body
Understand implications of new regulatory requirements and cascade them to all relevant stakeholders, products and Quality System
Responsible for preparation and submission of global regulatory applications, as well as internal regulatory file documentation
Support Product development projects from Regulatory perspective – establish regulatory deliverables, accompany a project team throughout the project and review and sign- off on product design control documentation for compliance with applicable regulations
Support documentation legalization that is needed for international submissions (notarization and apostil)
Support with FSC issuing and update
Work with Israeli MOH/ AMAR on new product registrations and update to current registrations
Maintenance of current MDD Tech Files with changes to products and changes to Regulations
Partner with the Regulatory Integration team on different regulatory tasks
Support audits (both external & internal) presenting Regulatory materials and with Regulatory inquiries
Support a work environment of continuous improvement that supports BSC’s Quality Policy, Quality System and the appropriate regulations for the area they support
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

Required Qualifications:

Bachelor’s degree, preferably in a scientific or technical discipline
At least 8 years' experience in the medical device industry (FDA, CE, International Regulations); if in Regulatory – 6 years
Working knowledge of design control documentation/requirements required
Excellent written & verbal English
Previous experience working with different PLM & ERP systems, Microsoft Office
Effective research and analytical skills

Requisition ID: 589305

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!

Job Segment: Regulatory Affairs, Compliance, Law, Product Development, Medical Device, Legal, Research, Healthcare