Offer summary

Qualifications:

8-10 years of regulatory affairs or relevant experience with a Bachelor’s degree (B.A./B.S.) required, or 6 years with a Master’s or advanced degree., Experience leading or authoring 510k or MDR submissions is required., Familiarity with global medical device regulations and standards such as ISO 13485, ISO 14971, and GDPR is highly preferred., Strong project management, problem-solving, organizational, and communication skills are essential..

Key responsabilities:

Develop global regulatory strategies for new and modified medical devices, including SaMD and wearable devices.

Prepare and submit international and domestic regulatory submissions to meet established timelines.

Collaborate with cross-functional teams to provide regulatory guidance and address compliance issues.

Interact with regulatory authorities to ensure submission approvals and maintain regulatory compliance throughout the product lifecycle.

Job description

Boldly innovating to create trusted solutions that detect, predict, and prevent disease.

Discover your power to innovate while making a difference in patients' lives. iRhythm is advancing cardiac care…Join Us Now!

At iRhythm, we are dedicated, self-motivated, and driven to do the right thing for our patients, clinicians, and coworkers. Our leadership is focused and committed to iRhythm’s employees and the mission of the company. We are better together, embrace change and help one another. We are Thinking Bigger and Moving Faster.

About this role:

iRhythm is currently seeking an experienced Staff Regulatory Affairs Specialist. This can be a remote or local position and an opportunity to be at the forefront of medical wearable and artificial intelligence technologies that are making a difference with patient outcomes and better healthcare. As a Staff Regulatory Affairs Specialist with a fast growing, AI software and wearable hardware medical device company, you will be responsible for working with cross functional teams to assess and develop global product registration strategies, help guide project teams from preparation to submission and through successful dossier reviews with global regulatory agencies to gain and maintain international product registrations. You will independently organize regulatory information and apply advanced regulatory expertise to guide cross-functional partners through strategic and creative thinking. Our work environment is fast-paced, with a collaborative atmosphere. Most of all, we are passionate about delivering innovations that improve the quality of health care and the patient experience. We are looking for like-minded individuals to join our team today!

Specific job responsibilities include:

Develop sound global, regional, and multi-country regulatory strategies for new and modified medical devices such as SaMD, wearable patches and/or OTC devices
Provide regulatory intelligence to aid in market assessments and portfolio planning
Prepare international and domestic submissions/registrations to established timelines and company objectives (e.g.,510(k), Q-submissions, Technical Documentations)
Represent Regulatory Affairs on assigned projects and provide regulatory guidance to the cross-functional teams
Collaborate with cross functional partners in driving and implementing new process to address non conformances or remediation efforts.
Anticipate regulatory and related obstacles and emerging issues throughout the product lifecycle
Interact with regulatory authorities during the development and review process to ensure submission approval
Defining regulatory requirements on device labeling and review labeling content for compliance for global markets
Coordinate with international contacts on product changes, regulatory notifications and registration/license maintenance
Review and approve product design changes to maintain regulatory compliance for significant changes
Author or revise SOPs to improve regulatory compliance of the Quality System
Monitor impact of changing global regulations on submission strategies & registrations
Perform other regulatory-related duties as assigned.

About you:

>8-10 years of regulatory affairs or relevant experience with a Bachelor’s degree (B.A./B.S. required)
>6 years’ experience with Master’s or other advanced degree in a related field
Lead and/or author 510k or MDR submission experience required
Software as a medical device (SaMD) experience highly preferred
AI/ML experience on ECG, sleep and/or physiologic signal monitoring highly preferred
Wearable and OTC medical device experience preferred
Familiarity with global medical device regulations; 21 CFR 820, MDD/CMDR, EU MDR, ASIA PAC, LATAM, etc. highly preferred
Demonstrated understanding of ISO 13485, ISO 14971, ISO 10993, GDPR, HIPAA and other international regulations/directives/standards highly preferred
Product development experience highly preferred
Strong project management skills
Exceptional problem-solving skills
Exceptional organizational skills
Exceptional communication (written and oral) skills
Willingness to travel when required, up to 10%

What’s in it for you:

This is a regular full-time position with competitive compensation package, excellent benefits including medical, dental, and vision insurances (all of which start on your first day), health savings account employer contributions (when enrolled in high deductible medical plan), cafeteria plan pre-taxed benefits (FSA, dependent care FSA, commute reimbursement accounts), travel reimbursement for medical care, noncontributory basic life insurance & short/ long term disability. Additionally, we offer:

emotional health support for you and your loved ones
legal / financial / identity theft/ pet and child referral assistance
paid parental leave, paid holidays, travel assistance for personal trips and PTO!

iRhythm also provides additional benefits including 401(k) (with company match), an Employee Stock Purchase Plan, pet insurance discount, unlimited amount of LinkedIn Learning classes and so much more!

FLSA Status: Exempt

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Actual compensation may vary depending on job-related factors including knowledge, skills, experience, and work location.

Estimated Pay Range

$124,800—$181,700 USD

As a part of our core values, we ensure a diverse and inclusive workforce. We welcome and celebrate people of all backgrounds, experiences, skills, and perspectives. iRhythm Technologies, Inc. is an Equal Opportunity Employer. We will consider for employment all qualified applicants with arrest and conviction records in accordance with all applicable laws.

iRhythm provides reasonable accommodations for qualified individuals with disabilities in job application procedures, including those who may have any difficulty using our online system. If you need such an accommodation, you may contact us at taops@irhythmtech.com

About iRhythm Technologies
iRhythm is a leading digital healthcare company that creates trusted solutions that detect, predict, and prevent disease. Combining wearable biosensors and cloud-based data analytics with powerful proprietary algorithms, iRhythm distills data from millions of heartbeats into clinically actionable information. Through a relentless focus on patient care, iRhythm’s vision is to deliver better data, better insights, and better health for all.

Make iRhythm your path forward. Zio, the heart monitor that changed the game.

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