Regulatory Response - San Jose, CA

TikTok is seeking a Trust and Safety Risk Containment - Regulatory Response & Compliance Safety Specialist with Portuguese language proficiency to join its global team.The ideal candidate will have strong knowledge of compliance frameworks, digital safety regulations, and an anal ...

The Regulatory Response Team specializes in navigating trust & safety issues regulatory requirements compliance global laws mitigating risks related to geopolitical developments user-generated content timely response escalations coordinated action major global incidents. · Invest ...

+The Regulatory Response Team specializes in navigating trust & safety issues, regulatory requirements, and compliance with global laws. The team plays a critical role in mitigating risks related to geopolitical developments and user-generated content, while ensuring timely respo ...

The Regulatory Affairs · Specialist supports regulatory compliance activities by preparing assessments and submissions required for product clearances and approvals.Prepare and manage regulatory assessments... · ...

Ensures regulatory compliance by completing thorough assessments and completing the appropriate submissions pertaining to product clearances/approvals by FDA, Notified Bodies, and other regulatory bodies. Viewed as team regulatory resource. · ...

We are seeking a highly skilled and experienced professional to join our Regulatory Affairs team as Sr. Manager, Regulatory Affairs. · Bachelor's degree in a scientific or engineering discipline. · Minimum of 8 years of regulatory affairs experience in the medical device industry ...

The Regulatory Affairs Specialist supports regulatory compliance activities by preparing assessments and submissions required for product clearances and approvals. · ...

Position Summary · Our client is seeking a senior-level Statistical Programming Consultant to support audit and inspection readiness for upcoming EMA and BLA filings. This role will partner closely with the Senior Director of Statistical Programming and serve as a key contributor ...

We are seeking a highly skilled and experienced professional to join our Regulatory Affairs team as Sr. Manager, Regulatory Affairs. · ...

Vibra Travels is seeking a travel Physical Therapist for various locations. Key responsibilities include providing and directing physical therapy services, assessing treatment plans, managing staff under physicians orders, and ensuring compliance with regulatory standards. · Job ...

Ensures regulatory compliance by completing thorough assessments and appropriate submissions pertaining to product clearances/approvals by FDA, Notified Bodies, and other regulatory bodies. · ...

The Regulatory Affairs Specialist is a key partner to R&D, Quality, Manufacturing, and Marketing teams, · responsible for driving regulatory strategy and ensuring compliance with global medical device regulations. · Develop regulatory strategies for new product introductions and ...

This is a full-time Director of Global Regulatory Affairs role based in San Jose, CA. The candidate will develop and implement regulatory strategies for global compliance. · ...

Good Samaritan Health Center, a leader in providing quality healthcare to underserved communities, is seeking a dedicated Director of Nursing to oversee our nursing department. This position is pivotal in ensuring that our mission of holistic health and wellness outcomes are met ...

Collaborates and executes regulatory strategies for global registrations and compliance activities. · ...

We are seeking a Regulatory Affairs Director to lead our regulatory strategies for digital pathology products, imaging devices, and AI/ML-based medical software. · This role will oversee global regulatory preparation and submissions (EU MDR/IVDR, Canada, Australia) while ensuring ...

The Regulatory Affairs Specialist prepares and documents regulatory submissions to government agencies. They work on problems of diverse scope where analysis of situations or data requires a review of identifiable factors. · ...

As a Principal Specialist in International Regulatory Affairs at Stryker Corporation, you will shape global regulatory strategies that accelerate access to medical technologies while protecting patients and communities worldwide. · ...

+Job summary · Responsible for the preparation and documentation of regulatory submissions to government agencies. Coordinates and supports the preparation of moderately complex regulatory submissions required for worldwide registration of products outside the U.S. and EU.Collabo ...

+ Lead U.S. FDA submissions including 510(k), De Novo, PMA, Q-Sub meetings, responses, amendments, · and technical documentation. · + Develop and execute regulatory strategies for digital pathology products, · imaging devices, · and AI/ML-based medical software.,+ Ensure complian ...