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#213848

Quality, Regulatory, Safety and Trust Specialist

Remote from Silicon Valley
Date:

Overview

Placement Type:

Temporary

Salary:

$96.72-107.47 Hourly

Start Date:

Nov 2, 2026

Aquent, a global leader in talent solutions, is partnering with a pioneering technology company at the forefront of innovation. This organization is dedicated to developing advanced solutions that prioritize safety, reliability, and trust, shaping the future of various industries. Join a team that values rigorous standards and groundbreaking approaches, making a tangible impact on cutting-edge technologies and operational excellence.

This is an exceptional opportunity to step into a pivotal role where your expertise will directly influence the integrity and efficiency of critical operations. As a key contributor, you will drive strategic initiatives, solve complex regulatory challenges, and ensure the highest standards of quality and compliance are met. Your work will directly contribute to the safety and seamless functioning of advanced systems, playing a crucial role in the continuous improvement and success of high-stakes projects. You’ll be at the forefront of defining best practices, collaborating with diverse teams, and shaping the regulatory landscape for innovative technologies.

What You’ll Do:

  • Provide expert guidance on design and analysis for complex projects, establishing regulatory frameworks and identifying potential risks and implications, while mentoring teams on critical trade-off decisions.
  • Facilitate early identification of risk elements for specific projects, developing and implementing contingency plans in collaboration with project teams.
  • Anticipate regulatory responses through scenario planning, communicating risks, and advising on regulatory management and courses of action for projects.
  • Establish and manage internal compliance processes, driving accountability, securing resources, and ensuring alignment with compliance and privacy policies.
  • Identify opportunities for and implement process improvements, including automation, and promote the adoption of new processes.
  • Conduct and analyze regulatory research to inform strategy, collaborating on regulatory strategies and resolving complex issues with minimal guidance.
  • Drive the preparation, planning, coordination, execution, and ongoing maintenance of regulatory submissions, ensuring quality and compliance.
  • Serve as the regulatory expert on cross-functional teams, evaluating submission management processes and sharing best practices.
  • Interpret existing regulations and guidance documents, building internal advocacy networks across various departments.
  • Understand political processes and their impact on public policy and regulatory laws.
  • Identify present and future unmet quality, regulatory, and compliance needs, generating novel approaches and creating scalable solutions.
  • Contribute domain expertise to regulatory, quality, clinical, product, design, and engineering teams.
  • Plan, coordinate, prepare, and execute meetings with regulatory agencies, facilitating communication and reviews.
  • Analyze data from events with extended recovery times to understand root causes, collaborating with cross-functional stakeholders and vendors.
  • Synthesize recurring issues across events to propose and implement fixes, driving continuous improvement initiatives.
  • Partner with vendors and internal teams to pinpoint process breakdowns and drive corrective actions within end-to-end processes.
  • Contribute to the population of key weekly reports and communications for executive audiences.

What You’ll Bring:

Required Skills & Qualifications:

  • Proficiency in registration and auditing processes.
  • Exceptional communication and influence skills.
  • Strong understanding of information governance.
  • Demonstrated project scoping and execution capabilities.
  • Expertise in regulatory compliance.
  • Proven risk management abilities.
  • Knowledge of standards, regulations, and reporting.
  • Solid project/program management skills.
  • Domain-specific knowledge and skills relevant to quality, regulatory, safety, and trust.
  • Technical, clinical, and partner knowledge.
  • Commitment to product excellence.
  • Strong business acumen.

Preferred Skills & Qualifications:

  • Experience in process auditing, particularly within supply chain or logistics, to identify and address inefficiencies.
  • Prior experience in vendor management, focusing on issue resolution and collaboration.
  • Adeptness at quickly learning and utilizing complex technical tools.

Client Description

Join one of the world’s most iconic technology visionaries, consistently recognized as a global leader in digital innovation. Our client offers a high-energy, collaborative environment where you will work alongside some of the industry’s brightest minds. This is a unique opportunity to gain experience within a multi-billion dollar tech giant, contributing to high-visibility projects that influence how the world connects and learns. For professionals looking to elevate their career, there is no better place to build your portfolio and witness large-scale innovation in action.