Recent Searches

You haven't searched anything yet.

2 Senior Specialist, Regulatory Affairs Jobs in Chelmsford, MA

SET JOB ALERT
Details...
Zoll Medical Corporation
Chelmsford, MA | Full Time
$89k-114k (estimate)
3 Weeks Ago
ZOLL LifeVest
Chelmsford, MA | Full Time
$101k-131k (estimate)
3 Months Ago
Senior Specialist, Regulatory Affairs
$89k-114k (estimate)
Full Time 3 Weeks Ago
Save

Zoll Medical Corporation is Hiring a Senior Specialist, Regulatory Affairs Near Chelmsford, MA

Resuscitation, ZOLLMED.com
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!
Job SummaryDevelop, 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 DemandsThe 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.
All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.

Job Summary

JOB TYPE

Full Time

SALARY

$89k-114k (estimate)

POST DATE

06/10/2024

EXPIRATION DATE

07/08/2024

WEBSITE

zoll.com

HEADQUARTERS

PITTSBURGH, PA

SIZE

1,000 - 3,000

FOUNDED

1983

TYPE

Private

CEO

CARMEN MELTON

REVENUE

$500M - $1B

Related Companies
About Zoll Medical Corporation

ZOLL designs, manufactures and markets medical devices and medical software.

Show more

Zoll Medical Corporation
Full Time
$88k-122k (estimate)
Just Posted
Zoll Medical Corporation
Full Time
$159k-198k (estimate)
2 Days Ago

The job skills required for Senior Specialist, Regulatory Affairs include Regulatory Affairs, Verbal Communication, Innovation, etc. Having related job skills and expertise will give you an advantage when applying to be a Senior Specialist, Regulatory Affairs. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Senior Specialist, Regulatory Affairs. Select any job title you are interested in and start to search job requirements.

For the skill of  Regulatory Affairs
Katalyst Healthcares & Life Sciences
Full Time
$74k-96k (estimate)
4 Months Ago
Show more

The following is the career advancement route for Senior Specialist, Regulatory Affairs positions, which can be used as a reference in future career path planning. As a Senior Specialist, Regulatory Affairs, it can be promoted into senior positions as a Regulatory Affairs Specialist III that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Senior Specialist, Regulatory Affairs. You can explore the career advancement for a Senior Specialist, Regulatory Affairs below and select your interested title to get hiring information.