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Skills
Administrative Skillsunmatched
Auditingunmatched
Change Controlunmatched
Clinical Information Systemsunmatched
Clinical Trialunmatched
Code of Federal Regulationsunmatched
Computer Systemsunmatched
Contract Research Organization (CRO)unmatched
Corporate Policiesunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Document Managementunmatched
Documentationunmatched
Drug Developmentunmatched
FDA Requirementsunmatched
GCP (Good Clinical Practices)unmatched
GxPunmatched
ICH Regulationsunmatched
Maintain Complianceunmatched
Mentoringunmatched
People Managementunmatched
Project Planningunmatched
Quality Assuranceunmatched
Quality Managementunmatched
Quality Metricsunmatched
Regulationsunmatched
Regulatory Complianceunmatched
Standard Operating Procedures (SOP)unmatched
System Validationunmatched
Training/Teachingunmatched
Willing to Travelunmatched
Description
Job Summary:
The Quality Assurance Manager is responsible for ensuring compliance with company policies, GCP regulations, and other relevant requirements. This role involves managing audits, document creation, CAPA management, and communication to meet quality objectives. The QA Manager reports to the Director of Quality.
Responsibilities:
Write, revise, and review SOPs, policies, and quality documentation
Provide guidance on non-conformance situations and investigations
Communicate compliance requirements at all levels
Represent the organization in quality-related presentations
Support inspection readiness and host audits
Develop quality systems to enhance compliance
Implement quality management plans for projects
Manage and host sponsor audits
Maintain annual audit plans and regulatory knowledge
Develop quality indicators and metrics
Provide GCP training sessions
Manage the electronic Quality Management System
Schedule Service Provider Qualifications
Oversee Computer System Validation and audits on projects
Act as QA Representative on clinical studies
Qualifications:
2 to 3 years of ZenQMS administration experience
3 years of experience in CSV/Change Control Management
3 to 5 years of experience in hosting sponsor audits
Experience in a CRO environment
Bachelor''s or advanced degree in science or related field with 8+ years in Quality
Knowledge & Skills Requirements:
Knowledge of FDA regulations, ICH-GCPs, and worldwide regulatory guidelines
Ability to interact with sponsors, mentor, and manage audit findings
Experience in developing quality systems and writing SOPs
Familiarity with clinical development software and 21CFR Part 11