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- Over 2.9 billion monthly active users across platforms
- Headquartered in Menlo Park, California
- Valued at over $800 billion
- Significant investments in Oculus and AR/VR technology
Meta (formerly Facebook) is a leading technology company focused on building the metaverse, with over 2.9 billion monthly active users across its platforms, including Facebook, Instagram, and WhatsApp. Headquartered in Menlo Park, California, Meta has invested heavily in virtual reality and augmente...
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Regulatory Affairs Specialist • Mid-Level
Overview
Meta is seeking a Regulatory Affairs Specialist to develop and execute regulatory strategies for medical devices. You'll manage product submissions for novel hardware and software as a medical device (SaMD) products. This role requires expertise in regulatory strategy and approvals.
Job Description
Who you are
You are an experienced regulatory affairs professional with a strong background in medical devices. You have a proven track record of developing and executing regulatory strategies that ensure compliance with global regulations. Your expertise in regulatory submissions and approvals enables you to effectively partner with cross-functional teams to launch innovative medical devices.
You possess a deep understanding of the regulatory landscape for medical devices, particularly in the context of consumer electronics and wearables. Your ability to navigate complex regulatory requirements allows you to provide valuable insights and guidance to your team. You are detail-oriented and have excellent communication skills, which help you articulate regulatory strategies to stakeholders.
What you'll do
In this role, you will be responsible for developing regulatory strategies for novel hardware and software as a medical device (SaMD) products. You will manage product submissions to ensure timely approvals and compliance with international regulations. Collaborating with cross-functional teams, you will enable the successful launch of regulated medical devices, particularly in the expanding portfolio of wearables and AI products.
You will apply your subject matter expertise to assess regulatory risks and develop mitigation strategies. Your role will involve staying updated on regulatory changes and trends that may impact product development and market access. You will also be responsible for preparing and reviewing regulatory documentation, ensuring that all submissions meet the necessary requirements.
What we offer
At Meta, you will be part of a dynamic team focused on innovation in the medical device space. We offer competitive compensation and benefits, along with opportunities for professional growth and development. Join us in shaping the future of healthcare technology through cutting-edge consumer electronics and AI solutions.
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