ZOLL Medical Corporation Logo

ZOLL Medical Corporation

Senior Specialist, Regulatory Affairs

Posted 10 Days Ago
Be an Early Applicant
Remote
Hiring Remotely in MA, USA
102K-152K Annually
Senior level
Remote
Hiring Remotely in MA, USA
102K-152K Annually
Senior level
Develops and leads regional regulatory strategies for new and sustaining medical device products. Responsibilities include preparing IDE, 510(k), PMA, Technical File, and Design Dossier submissions; providing regulatory guidance to cross-functional teams; supporting risk assessment, audits, compliance, product development, and commercialization; monitoring regulatory changes; and coordinating internal and external resources.
The summary above was generated by AI
Acute Care Technology

At ZOLL, we're passionate about improving patient outcomes and helping save lives.
We provide innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and treat patients suffering from serious cardiopulmonary and respiratory conditions.
The Acute Care Technology division of ZOLL develops and delivers innovative lifesaving products and software solutions to EMS, hospital, public safety, and military customers globally. Our dedicated employees take pride in their commitment to improving patient outcomes while delivering world-class customer service.
At ZOLL, you won’t just have a job. You’ll have a career—and a purpose.
Join our team. It’s a great time to be a part of ZOLL!

Open to Hybrid / Remote
Job Summary
Develop, implement, and lead the regulatory regional strategy, in alignment with company goals, for new and sustaining ZOLL Resuscitation products and features.
Essential Functions

  • Develop and successfully implement regional regulatory strategies for new and sustaining products/features that result in device approval.
  • Ensure project team colleagues, line management, and key stakeholders are apprised of developments that may impact regulatory success, exercising sound judgement and communicating in a professional and timely manner.
  • Provide strategic regional regulatory perspective during the development, review, and approval of internal and external documentation to support the development and commercialization of assigned product(s).
  • Work with RA regional and product teams to ensure that regulatory requirements are appropriately considered and accounted for in programs and projects.
  • Author and prepare submittals of IDEs, 510(k), PMAs, Technical Files or Design Dossiers, and other pertinent regional device applications.
  • Work with management on risk assessment and regulatory compliance.
  • Support Cross-Functional NPI Project Teams and provide regulatory guidance.
  • Maintain current knowledge of regulations and guidance and collaborate with product teams on approvals and disseminate information and generate potential strategies with teams.
  • Lead, support, and coordinate with internal and external resources to meet audit and compliance requirements.
  • Support a culture of continuous improvement by promoting best practices, fostering innovation, and recognizing and celebrating achievements as well report on key performance indicators (KPIs) to track the progress and impact of continuous improvement efforts.

Required/Preferred Education and Experience

  • Bachelor's Degree required
  • Advanced Degree preferred
  • 5+ years of regulatory affairs experience preferably in the medical device industry, with proven experience in electro-mechanical products required
  • Regulatory Affairs Certification Preferred

Knowledge, Skills and Abilities

  • Experience building regulatory strategies to support successful regulatory affairs team.
  • Proven written and verbal communication skills to interface with a variety of stakeholders.
  • Ability to create action plans and project deliverables.
  • Supports team members in the preparation of suitable written responses to Regulatory Inquiries.
  • Experience in the electro cardiology or defibrillation/respiratory space preferred.

Travel Requirements

  • Requires travel (~5% - 10%)

Physical Demands
The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job.

  • Standing - Occasionally
  • Walking - Occasionally
  • Sitting - Constantly
  • Talking - Occasionally
  • Hearing - Occasionally
  • Repetitive Motions - Frequently

ZOLL is a fast-growing company that operates in more than 140 countries around the world. Our employees are inspired by a commitment to make a difference in patients' lives, and our culture values innovation, self-motivation and an entrepreneurial spirit. Join us in our efforts to improve outcomes for underserved patients suffering from critical cardiopulmonary conditions and help save more lives.

The annual salary for this position is:

$101,600.00 to $152,400.00

This position is eligible for an annual bonus in accordance with the company's bonus plan. Factors which may affect starting salary include geography, skills, education, experience, and other qualifications of the successful candidate. Details of ZOLL's comprehensive benefits plans can be found at www.zollbenefits.com.

Applications will be accepted on an ongoing basis until this position is filled. For fully remote positions, compensation will comply with all applicable federal, state, and local wage laws, including minimum wage requirements, based on the employee’s primary work location.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, disability, or status as a protected veteran.

ADA: The employer will make reasonable accommodations in compliance with the Americans with Disabilities Act of 1990.

ZOLL Medical Corporation Parsippany, New Jersey, USA Office

Parsippany, United States

Similar Jobs

3 Days Ago
Remote
US
92K-138K Annually
Senior level
92K-138K Annually
Senior level
Other
Leads complex global regulatory projects for medical devices, including regulatory strategy, product submissions, market approvals, post-market changes, labeling, claims, audits, and responses to regulatory agencies. Evaluates technical evidence against regulations and standards, guides cross-functional teams, manages project timelines, monitors regulatory changes, and supports ongoing compliance. Requires at least four years of medical device regulatory affairs experience and expertise with FDA regulations, 510(k) submissions, and CE Technical Files.
Top Skills: 510(K) SubmissionsCe Technical FilesFda Regulations
One Month Ago
Remote
United States
128K-178K Annually
Senior level
128K-178K Annually
Senior level
Artificial Intelligence • Information Technology • Machine Learning • Marketing Tech • Software • Biotech • Design
Lead regulatory strategy and operations for SaMD products across development, submission, launch, and post-market. Manage regulatory documentation, change assessments, registrations, UDI, inspection readiness, and regulatory intelligence. Coordinate cross-functional stakeholders to ensure compliant filings, maintain trackers, and improve processes and tools for scale.
Top Skills: 510(K)De NovoDocument Control SystemsEqmsEu MdrFda Medical Device RequirementsIec 62304Iso 13485Iso 14971SamdSubmission Management ToolsUdi
11 Minutes Ago
Remote
US
170K-200K Annually
Entry level
170K-200K Annually
Entry level
Enterprise Web • Fintech • Marketing Tech • Software
Leads Unanet’s internal data strategy and architecture for enterprise AI. Defines the shared data foundation, target architecture, governance standards, roadmap, and reusable approaches for AI assistants, agents, and workflows. Evaluates platforms and integration options, validates technical solutions, and coordinates IT, Security, Legal, Engineering, business owners, and system specialists. Advises senior leaders, establishes data quality and stewardship requirements, and helps determine when data is ready to support scalable AI initiatives.
Top Skills: Artificial IntelligenceCloud Data PlatformsData GovernanceData IntegrationData LineageData ModelingData QualityGroundingIdentity And PermissionsMetadataMonitoringRetrieval

What you need to know about the NYC Tech Scene

As the undisputed financial capital of the world, New York City is an epicenter of startup funding activity. The city has a thriving fintech scene and is a major player in verticals ranging from AI to biotech, cybersecurity and digital media. It also has universities like NYU, Columbia and Cornell Tech attracting students and researchers from across the globe, providing the ecosystem with a constant influx of world-class talent. And its East Coast location and three international airports make it a perfect spot for European companies establishing a foothold in the United States.

Key Facts About NYC Tech

  • Number of Tech Workers: 549,200; 6% of overall workforce (2024 CompTIA survey)
  • Major Tech Employers: Capgemini, Bloomberg, IBM, Spotify
  • Key Industries: Artificial intelligence, Fintech
  • Funding Landscape: $25.5 billion in venture capital funding in 2024 (Pitchbook)
  • Notable Investors: Greycroft, Thrive Capital, Union Square Ventures, FirstMark Capital, Tiger Global Management, Tribeca Venture Partners, Insight Partners, Two Sigma Ventures
  • Research Centers and Universities: Columbia University, New York University, Fordham University, CUNY, AI Now Institute, Flatiron Institute, C.N. Yang Institute for Theoretical Physics, NASA Space Radiation Laboratory

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account