Quality Assurance Manager

7Seventy; California, Northern (MO, KY); Hybrid; USD 85,000 - 175,000; Full time

Benefits offered by this job

Bonus eligibility

Benefits package

Job summary

7Seventy is seeking a Quality Assurance Manager to provide independent oversight of clinical trial activities, processes, and documentation in the United States. The role ensures regulatory compliance, internal procedures, and quality standards while supporting continuous improvement across clinical operations.

The position requires 4-7+ years in QA or related fields, with supervisory experience preferred. You will maintain QA systems, develop SOPs, and lead audits and CAPA processes in a

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.
• Excellent communication and cross-functional collaboration skills.

Responsibilities

• 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.
• 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.

Skills

Quality assurance

GxP

ICH-GCP

FDA regulations

QMS

Microsoft Office

Communication

Independent judgment

Education

Bachelor’s degree in a scientific discipline

Tools

Microsoft Office

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