Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Regulatory Affairs Specialist I

Boston Scientific Corporation

Regulatory Affairs Specialist I

Work mode: Hybrid Onsite Location(s): American Free Zone, San Franci, H, CR Additional Locations: Costa Rica-Heredia

About the role: The Regulatory Affairs Specialist I supports Global Regulatory Affairs Operations by executing critical regulatory processes that help maintain compliance with global medical device regulations and business requirements. This role collaborates with divisional and country regulatory specialists, and cross-functional partners to support Notified Body activities, regulatory certificates, vendor invoicing, translation services, and regulatory information management.

Work Mode At Boston Scientific, we value collaboration and synergy. This hybrid role is based in Heredia, Costa Rica and requires being on-site at least three days per week.

Responsibilities:

  • Notified Body Support Support Notified Body activities by tracking requests, coordinating responses, managing regulatory deliverables, and following up on related commitments and stakeholder actions.
  • Maintain accurate and current Notified Body records, trackers, and supporting documentation in uTrack and other applicable regulatory systems.
  • Vendor and Translation Management Own regulatory vendor invoicing activities, including invoice tracking, reconciliation, payment follow-up, and issue resolution. Coordinate translation requests with external vendors and internal stakeholders to ensure timely delivery of completed regulatory documents.
  • Regulatory Systems and Process Improvement (Utrack) Maintain regulatory records, databases, trackers, and supporting documentation to support data accuracy, traceability, and compliance. Monitor operational requests and commitments, identify risks or gaps, escalate issues as appropriate, and support improvements that increase process efficiency and reliability.

Minimum Qualifications: Bachelor's degree in a scientific, technical, business, healthcare, or related field, or equivalent experience. 0-2 years of experience in Regulatory Affairs, Quality, Healthcare, Finance Operations, or a related discipline. Strong organizational, analytical, and problem-solving skills. Excellent written and verbal communication skills. Ability to effectively manage multiple priorities and deadlines. Proficiency with Microsoft Office applications, including Excel, Word, PowerPoint, and Teams.

Preferred Qualifications: Experience with regulatory operations, medical device compliance, or quality systems. Knowledge of Notified Body processes and regulatory certificate management. Experience with SAP, Ariba, uTrack, SharePoint, eRIM, Rimsys, or similar systems. Familiarity with FDA, EU MDR, ISO 13485, or international medical device regulations. Experience managing vendor relationships, invoicing processes, and translation services.

Requisition ID: 634315

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!

Benefits • Life-Work Integration • Community • Career Growth

At Boston Scientific, you will find a collaborative culture driven by a passion for innovation that keeps us connected on the most essential level. With determination, imagination, and a deep caring for human life, we're solving some of the most important healthcare industry challenges. Together, we're one global team committed to making a difference in people's lives around the world. This is a place where you can find a career with meaningful purpose—improving lives through your life's work.

Job Segment: Regulatory Affairs, Compliance, Medical Device, Developer, ERP, Legal, Healthcare, Technology

Vacancy posted 5 days ago
Similar jobs that could be interesting for youBased on the Regulatory Affairs Specialist I in United States vacancy
  •  ...Regulatory Submission Coordinator Direct or perform coordination and preparation of document packages for regulatory submissions related to the MiniMed separation from all areas of the company, internal audits, and inspections. Lead and compile all materials required... 
    Suggested
    Apprenticeship
    Local area
    Remote work

    LanceSoft

    United States
    1 day ago
  • $70k - $95k

     ...Job Title Industry Regulatory Affairs Job Type FT-Days Location REMOTE OPTION Salary $70,000 - $95,000 Job Description Responsibilities in this position will include: Supports preparation and maintenance of program annual reports, and may support... 
    Suggested
    Contract work
    Work at office
    Remote work

    KMR Search Group

    United States
    1 day ago
  •  ...Regulatory Affairs Specialist Role Type: Contractor Location: Remote micro1 is engaging Regulatory Affairs Specialists to contribute to a customer's project focused on AI innovation in regulatory documentation. In this role, you'll apply your expertise to help... 
    Suggested
    For contractors
    Remote work

    micro1

    United States
    2 days ago
  •  ...Regulatory Affairs Specialist We are seeking a detail-oriented and experienced Regulatory Affairs Specialist to join our team in Canada. The successful candidate will be responsible for ensuring compliance with Canadian regulatory requirements for our products, working... 
    Suggested
    Work at office
    Remote work

    MDA Edge

    United States
    4 days ago
  • $85k - $95k

     ...LivaNova is seeking a Regulatory and Clinical Specialist to support clinical evaluations and regulatory submissions for active implantable medical devices. The role requires solid experience in writing evaluation plans and reports, managing documentation processes, and... 
    Suggested
    Remote work
    Flexible hours

    LivaNova

    United States
    3 days ago
  •  ...Financial Affairs Specialist page is loaded## Financial Affairs Specialistlocations: İstanbul - Çamlıcatime type: Full timeposted on: Posted Todayjob requisition id: JR28826As proud bakers and chocolatiers and custodians of iconic global brands, we don’t compromise on... 
    Weekly pay
    Daily paid
    Local area

    pladis Foods Limited

    Turkey, NC
    2 days ago
  • The Compliance Specialist reports to the Director Legal, Compliance, Privacy & Security (“Director”) and has a key role in supporting the...  .... ~ Conduct research and develop written communication on regulatory requirements to ensure ongoing updates upon request. ~ Manage... 
    Contract work

    Cedent

    Houston, TX
    4 days ago
  • $80k - $95k

     ...Job Description Job Description Job Purpose The Regulatory Affairs Specialist is responsible for coordinating and executing routine regulatory activities that support the company’s worldwide medical device business. This position supports product registrations,... 
    Work at office
    Worldwide
    Weekend work
    Afternoon shift

    Nihon Kohden Orange Med

    Santa Ana, CA
    25 days ago
  •  ...goal of delivering diagnostic solutions to some of the most critical questions in healthcare. Position Summary The Regulatory Affairs Specialist will support the preparation, review, and submission of regulatory documentation for medical device/IVDs products,... 
    Flexible hours

    CorDx

    Alpharetta, GA
    25 days ago
  •  ...Job Description Job Description Medical Device Industry Kelly Science is seeking an experienced Regulatory Affairs Specialist to support regulatory strategy, submissions, and ongoing compliance for a medical device organization. This position is ideal for a hands-... 
    Temporary work
    Local area

    Kelly Services

    Goose Creek, SC
    8 days ago
  •  ...Job Responsibilities: Utilize the Regulatory Information Management System (RIMS) to manage data accuracy, integrity, and process efficiency; perform data analysis and manage submission/document and data uploads and verification; generate RIMS extracted reports to... 

    SGS Consulting

    New Jersey
    more than 2 months ago
  •  ...Hybrid role in Earth City, MO office Job Title Regulatory Affairs Specialist Job # US20130 Requisition Type Regular Function Legal & Risk State/Province Missouri City St. Louis Region US Posting Start Date Aug-16-2026 Division Information... 
    Full time
    Work at office
    Worldwide

    Spectrum Brands

    Saint Louis, MO
    a month ago
  •  ...Job Description Job Description Description: JOB PURPOSE: · Execute on regulatory strategy of De Novo submissions for AI/ML-based Software as a Medical Device (SaMD) product, including AidaBreast. · Serve as regulatory lead for novel oncology diagnostic technologies... 

    Prelude Corporation

    Laguna Hills, CA
    25 days ago
  •  ...Peregrine Team is seeking a Regulatory Affairs Specialist to support global regulatory submissions and ensure compliance across pharmaceutical products. This role will work closely with cross-functional teams to support product approvals and lifecycle management. Key... 
    Full time

    Peregrine Team

    Raleigh, NC
    15 days ago
  •  ...every senior and their family thrive through personalized and holistic health. Position Summary: The Compliance & Regulatory Affairs Specialist reporting directly to the Associate General Counsel is responsible for building, managing, and continuously improving... 
    For contractors
    Work at office

    Dover Health

    Saint Louis, MO
    25 days ago
  • $75k - $85k

     ...like solving hard problems alongside people who do the same, you'll fit right in. About The Role We're looking for a Regulatory Affairs Specialist to support compliance across our dietary supplement product lines. Reporting to the Regulatory Affairs Manager, you'll... 
    Full time
    Fixed term contract
    Remote work
    Work from home

    Scale Media

    Burbank, CA
    18 days ago
  •  ...Job Description Job Description Regulatory Affairs Specialist requires: ~1-3 years experience in regulatory affairs field of Laundry and detergents or CPG products. ~ Knowledge of federal and state statutes and regulations related to pesticide registration (required... 
    Work at office
    Local area

    Globalchannelmanagement

    Trumbull, CT
    29 days ago
  • $55 - $60 per hour

     ...Job Title: Regulatory Affairs Specialist IV Location: Sunnyvale, California Type: 6 month contract Compensation: $55-60/hour depending on qualifications Work Model: Hybrid – 3 days onsite Hours: 40.0 Overview Lead regulatory strategy and submissions... 
    Contract work
    Temporary work
    Local area

    System One

    Sunnyvale, CA
    more than 2 months ago
  •  ...dynamic and growing team with established products and an entrepreneurial mindset. Role Description:   dThe Regulatory Affairs (RA) Specialist is responsible for supporting global regulatory submissions and compliance activities to ensure medical device... 
    Internship
    Work at office
    Worldwide

    Spectrum Vascular

    Bridgewater, NJ
    17 days ago
  • $100k - $105k

     ...in recruiting top talented professionals for Southern California's Scientific community. We are currently looking for a Regulatory Affairs Specialist to work for a leading Greater Los Angeles area medical device company. Salary : $100-105k Responsibilities:... 

    BioPhase Solutions

    Los Angeles, CA
    23 days ago
  •  ...Job Description Job Description Job Title : Regulatory Affairs Specialist Reports To : VP Quality & Regulatory Affairs Position Status : Exempt Description: Broadly recognized as a Regulatory Expert in US, EU, and other regional Regulatory filings.... 
    Work experience placement
    Worldwide

    Reva Medical LLC

    San Diego, CA
    3 days ago
  •  ...local regulations on facilities/products registration, air and water pollution, waste disposal, and chemical releases; deals with regulatory agencies, develops compliance strategies, directs related training efforts. Major Functional Objectives: 1.) To Contact and... 
    Temporary work
    Local area

    Carlsbad Tech

    Carlsbad, CA
    a month ago
  • $33 per hour

     ...Job Description Job Description Regulatory Affairs Specialist (Food & Beverage)? Remote ? Up to $33/hour (Contract) ? 12-Month Contract ? Potential Temp-to-Perm Opportunity Permanent Salary Upon Potential Conversion: $60,000–$70,000 annually (based on... 
    Permanent employment
    Contract work
    Temporary work
    Work at office
    Local area
    Remote work

    Zing! Recruiting

    Saddle Brook, NJ
    25 days ago
  •  ...Description Job Description Job Description This position of Regulatory Specialist reports directly to the Vice President of Quality Control &...  ...include:   ~ Interpretation of regulations and legal affairs (domestic and international) for the flavor industry... 
    Work at office

    Coda Staffing

    Totowa, NJ
    29 days ago
  • $50 - $80 per hour

     ...Role Overview Apply regulatory affairs expertise to help train next-generation AI systems for regulatory documentation. You will contribute high-quality, real-world evaluations and feedback that shape how models reason about clinical submissions, agency requests, and... 
    Hourly pay
    For contractors
    Remote work

    SaidGig

    United States
    a month ago
  •  ...Job Description Job Description Pesticides Regulatory Affairs Specialist needs 5 years of experience in pesticide product registration; or equivalent combination of education and experience, including preparation and submission of pesticide registration applications... 

    Globalchannelmanagement

    Trumbull, CT
    29 days ago
  • $107.2k - $160.8k

     ...he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality system and applicable regulatory requirements. This position will also prepare, monitor, and communicate status of regulatory... 
    Work at office
    Local area
    Immediate start
    Flexible hours

    Coloplast A/S

    Minneapolis, MN
    a month ago
  •  ...Job Description Job Description Regulatory Affairs Specialist (Biologics) Employment Type: 6-Month Contract Location: Fully Remote Position Overview We are seeking an experienced Regulatory Affairs Specialist to support the Biologics division... 
    Contract work
    Local area
    Remote work

    Medix

    Anaheim, CA
    4 days ago
  •  ...Job Title: Regulatory Affairs Specialist II OnSite @Chaska location Mon-Fri 8 to 5 7:30 AM to 4:30 PM - Flexible Duration: 12 months on Contract Skills required for this position: 1. Regulatory experience in Medical Device... 
    Contract work
    Work experience placement
    Flexible hours

    Sunrise Systems

    Edison, NJ
    a month ago
  •  ...for ensuring that all products comply with applicable global regulatory requirements throughout their lifecycle-from development and registration to post-market surveillance. The Regulatory Affairs Specialist helps ensure regulatory compliance for diagnostics products with... 

    ELITechGroup Inc.

    Logan, UT
    4 days ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Regulatory Affairs Specialist I. Be the first to apply!