CA47I5-Privacy & Data Protection Specialist - C99 - Privacy Regulatory Specialist C99 - Privacy Regulatory Specialist - Seattle

This position is responsible for regulatory submissions required to market medical devices in both the U.S. and Europe. · Prepare regulatory submissions required to market medical devices in both the U.S. and Europe. · Support international product registrations. · ...

This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe. · ...

Description · How do you get items to customers quickly, cost-effectively, and—most importantly—safely, in less than an hour? And how do you do it in a way that can scale? Our teams of hundreds of scientists, engineers, aerospace professionals, and futurists have been working har ...

+ Regulatory compliance specialist responsible for managing state licensing and registrations. + · Possible 6 month contract with potential to extend or convert. · ++Manage state licensing and registrations. · Act as legal liaison. · Conduct regulatory monitoring. · ...

Manage state licensing and registrations by overseeing the end-to-end process. · Act as a legal liaison by collaborating closely with financial services attorneys. · Conduct regulatory monitoring by actively checking state agency portals. · Master e-submissions by becoming profic ...

This role is part of the global design and development teams supporting the Philips Oral Healthcare business unit, · which delivers power toothbrushes, power flossers and whitening solutions to millions of customers worldwide.This Regulatory Affairs Specialist will assist with im ...

As part of the continued growth and innovation of our Capital Project Delivery service offering, ERM has an opportunity for an experienced biologist/regulatory specialist to join our thriving global consulting firm in Seattle, WA, as a Managing Technical Consultant, Biologist/Reg ...

+ Develops and facilitates regulatory submissions for new products/solutions. · + Identifies potential regulatory approval risks based on changes in regulations... · + You're The Right Fit If you have a Bachelor's or Master's degree in Chemistry... ...

This is an opportunity to make an impact at ERM as a Managing Technical Consultant. · ...

Ready to Shape the Future of Power and Technology? · If you're a seasoned environmental leader who thrives on solving complex challenges and influencing the development of transformative projects, this is your opportunity to make an impact. · At ERM, we're not just delivering pro ...

Ready to Shape the Future of Power and Technology? · Lead environmental impact assessments and permitting efforts for marine and onshore environments under CEQA and NEPA. · ...

Ready to Shape the Future of Power and Technology? · If you're a seasoned environmental leader who thrives on solving complex challenges and influencing the development of transformative projects, this is your opportunity to make an impact. · ...

+Responsibilities:This position is responsible for the preparation of regulatory submissions required to market medical devices in both the U.S. and Europe... · Requirements: · B.S. degree or higher in a life science or technical discipline... · ...

We are seeking an experienced medical devices regulatory affairs professional to develop and execute regulatory strategies and manage product submissions for novel hardware and software as a medical device (SaMD) products for distribution into worldwide markets. · Act as the core ...

We are seeking an investigator in our Commercial Airplanes (BCA) Safety and Compliance Investigations (S&CI) team. This role involves leading teams tasked with performing detailed Root Cause Corrective Action (RCCA) investigations related to regulatory compliance issues. · ...

Role Overview · Crave InfoTech is looking for a highly experienced Senior SAP FI/CO Regulatory Specialist with strong expertise in FERC regulatory reporting and utility accounting to support a critical regulatory and financial reporting initiative. · This role requires a hands-on ...

The CMC Document Specialist supports the documentation activities for regulatory submissions for cell therapy products as part of the Technical Writing group in Pipeline and Product Lifecycle Strategy (PPLS).This role requires a strong focus on details and effective collaboration ...

We are seeking a Public Outreach & Education Specialist to support transportation and environmental projects through community engagement, stakeholder coordination, and educational initiatives. This role helps ensure that project information is effectively communicated, community ...

We are seeking a detail-oriented Permitting Specialist to support transportation and environmental planning projects. This role provides permit management, regulatory guidance, and project coordination for infrastructure initiatives, ensuring compliance with local, state, and fed ...

The Sr. Specialist Quality Systems is a full-time position responsible for providing oversight and guidance for assigned quality systems and compliance activities across the Cell Therapy Development and Operation (CTDO) at Dexter Corporate Office located in Seattle, Washington. · ...