Medical Devices, Regulatory Specialist
Meta
90k - 137k USD/year
Office
Burlingame, CA | New York, NY
Full Time
We're seeking a regulatory affairs specialist to join our medical devices compliance team. You will get to work on wearables and Software as a Medical Device (SaMD) applications for the US and worldwide approvals.
You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.Medical Devices, Regulatory Specialist Responsibilities
$९०,०००/year to $१,३७,०००/year + bonus + equity + benefits
Individual compensation is determined by skills, qualifications, experience, and location. Compensation details listed in this posting reflect the base hourly rate, monthly rate, or annual salary only, and do not include bonus, equity or sales incentives, if applicable. In addition to base compensation, Meta offers benefits. Learn more about benefits at Meta.
Equal Employment Opportunity Meta is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or other applicable legally protected characteristics. You may view our Equal Employment Opportunity notice here. Meta is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, fill out the Accommodations request form.
You will work on cutting-edge wearable technologies, including augmented reality glasses, wrist wearables, and other innovative devices.Medical Devices, Regulatory Specialist Responsibilities
- Interact directly with FDA and/or indirectly with international regulatory agencies on most projects/products at reviewer level. All significant issues will be reviewed with the manager
- Support regulatory compliance activities, including site registration, audits, post-market vigilance reporting, product recalls, etc., as needed
- Prepare FDA, European and Canada submissions for product changes as required to ensure timely approval for market release. Review significant regulatory issues with manager, as necessary, and resolve submission issues with engineering partners, geography regulatory partners, and regulatory agencies as needed
- Prepare regulatory strategies/plans and compliance requirements. Provide on-going support to project teams for regulatory issues and questions
- Bachelor’s degree in a scientific discipline or equivalent work experience
- 3+ years of industry experience in medical device regulatory affairs or related industry
- Experience working with minimal supervision and under general direction only
- Experience multitasking, supporting multiple projects, functioning on a global basis, prioritizing, conducting team meetings, and meeting project deadlines
- Experience with Food and Drug Administration
requirements, guidance documents, Active Medical Device Directive/EU MDR, ISO 14971, ISO 13485, and other global regulatory requirements and quality standards - Advanced degree in a scientific discipline (engineering, physical/biological or health sciences) or in Regulatory Affairs
- Regulatory Affairs Professionals Society Regulatory Affairs Certification
- Demonstrated experience in negotiation skills, authoring technical reports and submissions, and presenting to cross functional peers and leadership
$९०,०००/year to $१,३७,०००/year + bonus + equity + benefits
Individual compensation is determined by skills, qualifications, experience, and location. Compensation details listed in this posting reflect the base hourly rate, monthly rate, or annual salary only, and do not include bonus, equity or sales incentives, if applicable. In addition to base compensation, Meta offers benefits. Learn more about benefits at Meta.
Equal Employment Opportunity Meta is proud to be an Equal Employment Opportunity employer. We do not discriminate based upon race, religion, color, national origin, sex (including pregnancy, childbirth, reproductive health decisions, or related medical conditions), sexual orientation, gender identity, gender expression, age, status as a protected veteran, status as an individual with a disability, genetic information, political views or activity, or other applicable legally protected characteristics. You may view our Equal Employment Opportunity notice here. Meta is committed to providing reasonable accommodations for qualified individuals with disabilities and disabled veterans in our job application procedures. If you need assistance or an accommodation due to a disability, fill out the Accommodations request form.
Medical Devices, Regulatory Specialist
Office
Burlingame, CA | New York, NY
Full Time
90k - 137k USD/year
August 9, 2025