About this opportunity
7Seventy lists this Quality Assurance Manager opportunity in california, Missouri. Review the employer’s description below for duties, qualifications and application requirements.
Job description
This opportunity is for a Quality Assurance Manager to provide independent oversight of clinical trial activities, processes, and documentation. The role focuses on ensuring compliance with regulatory requirements, internal procedures, and quality standards while supporting continuous improvement across clinical operations.
This position operates in a fast-paced, collaborative environment and plays a key role in maintaining quality across internal teams, vendors, and clinical programs.
Job Type: Full-Time
Compensation: $85,000 - $175,000
What You’ll Do
Maintain up-to-date knowledge of GxP regulations and communicate relevant updates to stakeholders
Support implementation, maintenance, and oversight of the Quality Management System (QMS)
Develop, review, and maintain SOPs and quality documentation in alignment with regulatory requirements
Provide client-facing QA support, including development of quality documentation and compliance guidance
Establish and maintain quality standards, controls, and performance parameters across clinical programs
Ensure compliance with federal, state, local, and organizational regulations and policies
Implement and support Clinical Quality Assurance plans aligned with GCP standards
Lead and support audit and inspection readiness activities, including regulatory inspections
Plan and conduct internal and external audits, including vendor qualification and oversight
Oversee CAPA processes, including tracking, root cause analysis, and escalation of quality issues
Analyze quality metrics and trends to identify risks and support continuous improvement
Provide QA guidance to cross-functional teams and support interpretation of regulatory requirements
Review clinical and regulatory documents such as protocols, study reports, and summaries
Support development and delivery of training materials related to GCP and SOPs
Collaborate with clinical teams to investigate deviations, temperature excursions, and product complaints
Participate in QA budget planning and resource forecasting
Develop and report GCP quality metrics across the organization
Support additional projects and responsibilities as needed
Qualifications
4-7+ years of experience in quality assurance or a related field
Supervisory experience is preferred
Strong knowledge of GxP, ICH-GCP, and FDA regulations
Experience working with Quality Management Systems (QMS)
Highly organized with the ability to manage multiple priorities
Proficiency with Microsoft Office tools (Outlook, Excel, PowerPoint, Word)
Strong attention to detail and ability to maintain confidentiality
Ability to exercise independent judgment and decision-making
Excellent communication and cross-functional collaboration skills
Education
Bachelor’s degree in a scientific discipline is preferred
Equivalent experience with a related degree may be considered
Foreign degrees should be supported by a U.S. equivalency evaluation if applicable
Additional Information
Compensation may vary based on experience and seniority level
Bonus eligibility and benefits package are included
Vaccination requirements may apply depending on client-specific guidelines
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Worksite address
california, MO, 65018, US
Who can apply
Review the original listing for work authorization, qualifications and employer requirements.