Lead quality initiatives, audits, and compliance programs to align with client and regulatory standards.
Analyze performance data and collaborate with cross-functional teams to implement process improvements.
Develop executive reports and tools to drive quality excellence and support operational accuracy.
The partner company operates in the US security and IT sector, focusing on quality and operational excellence. It maintains a dynamic, collaborative culture that values continuous improvement and client satisfaction.
Provide strategic quality oversight for global clinical operations, including decentralized clinical trials and patient-focused healthcare services.
Ensure compliance with global regulations, sponsor expectations, and established quality systems through risk management and continuous improvement.
Lead investigations, audits, and CAPA activities to support safe, efficient, and reliable clinical trial delivery.
The partner company is a mission-driven organization focused on improving access to healthcare solutions. They foster a supportive, inclusive, and collaborative work environment with a remote-first culture.
Lead the development and execution of a comprehensive QA strategy for nuclear projects across the full lifecycle.
Oversee supplier qualification, audits, and compliance with NRC regulations and ASME NQA-1 requirements.
Collaborate with cross-functional teams to embed a strong quality culture and support regulatory readiness.
We are focused on advancing clean energy through advanced nuclear development. We offer a collaborative culture centered on innovation, accountability, inclusion, and professional growth, with a growing team.
Lead implementation and improvement of quality management systems, including certifications. - Develop solutions for complex quality challenges and provide training on quality processes. - Conduct audits, manage non-conformance investigations, and drive continuous improvement.
The partner company is a technology-driven organization focused on safety, reliability, and continuous improvement. It operates globally and emphasizes quality management and operational excellence, with a culture of collaboration and innovation.
Lead the execution and continuous improvement of quality management systems to ensure compliance with FDA, ICH, GCP, and ISO 9001 standards.
Manage electronic Quality Management System (eQMS) including document control, CAPA, risk management, and audit processes.
Provide quality oversight for clinical trial activities and software development lifecycle, collaborating with cross-functional teams.
The partner company is a fast-growing healthcare and life sciences organization focused on improving clinical research. It values collaboration, curiosity, and continuous improvement, and supports teams through scalable systems and risk management.
Oversee GCP quality systems and provide QA leadership for global clinical operations including decentralized trials.
Lead investigations, CAPAs, risk assessments, and audits to ensure regulatory compliance.
Review clinical documentation, support vendor qualification, and mentor QA staff.
WEP Clinical partners with biopharmaceutical sponsors to deliver clinical trial services, home health, and market access solutions. With over 15 years of global experience across 150+ countries, the company fosters a collaborative and mission-driven culture.
Maintain and improve the Quality Management System (QMS) and support compliance with CMMI, CMMC, and ISO standards.
Support government contract compliance, coordinate audits, and manage documentation for contracts and IDIQ vehicles.
Develop dashboards and reports for compliance, audits, and PMO maturity metrics.
True Zero Technologies is a veteran-owned small business that focuses on enabling people and technology to drive quality outcomes. The company has been recognized as a Best Places to Work honoree and has appeared on the Inc. 5000 list of fastest-growing companies, reflecting its people-first culture and commitment to excellence.
Conduct health and safety compliance audits for construction sites.
Perform desktop review of site plans and client checklists.
Collaborate with client stakeholders and construction teams to ensure safe operational facilities.
Apex is a consulting and engineering firm that builds projects shaping communities and protecting the environment. They are a fastest-growing firm in the AEC industry with a collaborative culture that invests in employee development.
Provide operational and program support to safety leadership and regional teams by coordinating priorities and initiatives.
Maintain safety program trackers, compliance schedules, and reporting timelines for continuous improvement.
Administer safety management systems and coordinate training programs to ensure compliance and documentation.
Our partner company operates in the renewable energy and construction sectors, focusing on safety and compliance. They have a distributed team across the US and prioritize a strong safety culture.
Provide strategic leadership and oversight for GCP quality assurance activities supporting clinical development programs.
Lead the development, planning, and execution of GCP audits, including clinical sites, CROs, vendors, and internal processes.
Own regulatory inspection readiness and collaborate with cross-functional teams to ensure compliance with GCP standards.
Cogent Biosciences is a publicly traded biotechnology company focused on developing precision therapies for unmet medical needs. The company fosters a collaborative culture and is committed to advancing treatments for rare conditions.
Implement and maintain best-in-class quality systems in compliance with FDA, ICH, 21 CFR Part 11, and ISO 9001.
Foster a culture of quality excellence and continuous improvement across the organization.
Manage day-to-day activities of a lean, high-performing quality team and optimize workflows.
N-Power Medicine aims to reinvent drug development by transforming clinical trials through better integration with clinical practice. They are building a multi-disciplinary team with diverse expertise in healthcare, engineering, technology, and regulatory, sharing a core value of empowering community through generosity, curiosity, and humility.
Build, maintain, and continuously improve the company's Quality Management System (QMS) and oversee GxP CSV requirements.
Own the design and administration of the electronic QMS, including validation, document control, and compliance activities.
Lead internal audit and inspection-readiness programs, supporting regulatory inspections and promoting a culture of quality.
Loyal is a clinical-stage veterinary medicine company developing longevity drugs for dogs, targeting the underlying drivers of aging to delay disease and preserve quality of life. As a well-funded startup with teams of scientists, veterinarians, engineers, and creatives, it is pioneering the first FDA-approved lifespan extension medicine.