Job summary
Job post source
This job is directly from Meta
Job overview
The Medical Devices, Regulatory Specialist at Meta ensures regulatory compliance for wearable and Software as a Medical Device products, impacting global market approvals.
Responsibilities and impact
The role involves interacting with FDA and international regulatory agencies, supporting compliance activities like audits and recalls, preparing submissions for regulatory approvals, and developing regulatory strategies to support project teams.
Compensation and benefits
The position offers a salary range of $90,000 to $137,000 per year, plus bonus, equity, and benefits including health insurance and retirement plans.
Experience and skills
Candidates need a bachelor's degree or equivalent experience, 3+ years in medical device regulatory affairs, ability to multitask globally, and preferred qualifications include FDA and EU regulatory knowledge, advanced degrees, and Regulatory Affairs certification.
Work environment and culture
Meta values diversity, inclusion, and equal opportunity, fostering a supportive environment with accommodations for disabilities and leveraging AI in recruitment.
Company information
Meta is a leading technology company focused on social connection and immersive experiences through augmented and virtual reality, with popular apps like Facebook, Instagram, and WhatsApp.
Unique job features
The role involves working on cutting-edge wearable technologies including augmented reality glasses and wrist wearables, contributing to innovative medical device compliance.
Company overview
Meta, formerly known as Facebook, is a leading technology company specializing in social media, virtual reality, and digital advertising. They generate revenue primarily through advertising on platforms like Facebook, Instagram, and WhatsApp, leveraging user data to offer targeted ads. Founded by Mark Zuckerberg in 2004, the company rebranded to Meta in 2021 to reflect its focus on building the metaverse, a virtual shared space. Key historical moments include the acquisition of Instagram in 2012 and WhatsApp in 2014, significantly expanding their user base and market influence.
How to land this job
Position your resume to highlight your experience with medical device regulatory affairs, focusing on your knowledge of FDA, EU MDR, ISO 14971, and ISO 13485 standards, as these are critical for the role at Meta.
Emphasize your ability to manage regulatory submissions for wearable technologies and Software as a Medical Device (SaMD), showcasing your skills in preparing FDA, European, and Canadian submissions and navigating complex regulatory environments.
Apply through multiple channels including Meta's official careers page and LinkedIn to maximize your application visibility and ensure your resume reaches the right recruiters.
Connect with current Meta employees in the medical devices or regulatory compliance teams on LinkedIn; start conversations by referencing Meta’s innovative wearable tech projects or asking about their experience working on regulatory challenges for new technologies.
Optimize your resume for ATS by incorporating keywords like 'regulatory submissions,' 'FDA compliance,' 'ISO 13485,' 'wearable medical devices,' and 'post-market vigilance,' ensuring your resume passes automated screenings effectively.
Use Jennie Johnson's Power Apply feature to automate tailored applications, identify multiple application portals, and find LinkedIn connections, allowing you to focus your time on preparing for interviews and networking effectively.
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