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ZOLL Medical Corporation

Senior Specialist, Regulatory Affairs

Posted 2 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 San Jose, California, USA Office

San Jose, United States, 0

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