Quality Assurance Manager

Prinston Laboratories; Charlotte (NC); On-site; USD 130,000 - 160,000; Full time

Job summary

Prinston Laboratories seeks a Quality Assurance Manager for its pharmaceutical oral solid dosage facility in Charlotte, NC. You will oversee the Site Quality Management System, ensure cGMP compliance, manage document control, training, and market vigilance to maintain inspection readiness.

You will lead batch review and disposition, COA/CoC reviews, and CAPA programs, while driving risk-based investigations and continuous improvement across QA operations.

Qualifications

• Bachelor’s degree in a scientific discipline with advanced degree preferred.
• Minimum 6+ years of progressive QA/QMS experience in QA or related roles.
• Experience with cGMP, FDA regulations, and regulatory inspections.
• Strong knowledge of QMS, documents, data integrity, and CAPA processes.
• Proven ability to lead cross-functional projects and teams.

Responsibilities

• Oversee QA/QMS activities, SPC, APQR and QMR data analysis to support leadership decisions.
• Lead batch review, disposition, COA/CoC reviews and final batch release under applicable regulations.
• manage investigations for quality events, deviations and customer complaints using RCA.
• Define and implement CAPA, risk management, and compliance improvements.
• Maintain document control lifecycle and data integrity across the site.

Skills

Leadership

Communication

Analytical thinking

Project management

Cross-functional teams

Risk-based decisions

Time management

Quality assurance

Education

B.S. in Chemistry/Pharmacy/Engineering

Tools

TrackWise

Veeva Vault

MasterControl

SAP

Microsoft Office

Job description

Quality Assurance Manager – Pharmaceutical Oral Solid Dosage

Job Summary

The Quality Assurance Manager is responsible for the strategic oversight, execution, and continuous improvement of the Site Quality Management System (QMS), product disposition, document control, personnel training, and market vigilance (customer complaints) at our pharmaceutical manufacturing facility. This role ensures that all operations comply fully with current Good Manufacturing Practices (cGMP), US FDA regulations (21 CFR Parts 210, 211, and Part 11), ICH Q10, state regulations, and corporate compliance standards by maintaining an inspection-ready, fully qualified, and highly responsive manufacturing site.

Key Responsibilities

• Drive the compilation and advanced statistical modeling of data for the Annual Product Quality Review (APQR) and monthly QMRs, delivering actionable data-driven metrics to site executive leadership.
• Establish and champion the site's Statistical Process Control (SPC) program. Monitor and analyze critical quality attributes (CQAs) and critical process parameters (CPPs) using control charts to identify out-of-control trends before deviations occur. Apply Six Sigma tools (DMAIC, Gauge R&R, ANOVA, Capability Indices like Cp/Cpk) to lead cross-functional variance reduction projects, targeting systemic manufacturing defects and minimizing product variability.

2. Batch Review & Disposition Ownership

• Manage the site batch record review and product disposition process to ensure all incoming materials, WIPs and finished products meet established specifications prior to market distribution.
• Review and approve Certificates of Analysis, Certificates of Conformance (CoC), and final batch release documentation under 21 CFR 211.192.
• Direct the control, segregation, and disposition of quarantined, rejected, or reprocessed raw materials, intermediates, and finished solid dosage products based on rigorous statistical and scientific evaluations.

3. Quality Events, Deviations & Customer Complaints

• Lead and approve formal investigations for quality events and Customer Complaints (PQCs) by utilizing statistical analysis to implement.
• Implement risk management approaches to identify, mitigate and eliminate risk to the product quality.
• Drive the definition and timely execution of Corrective and Preventive Actions (CAPA) using advanced root cause analysis (RCA) tools to mitigate systemic equipment and market defect issues.

4. Document Management & GxP Records Lifecycle

• Oversee the site Document Control center. Manage the full lifecycle (authoring, formatting, workflows, multi-layer approvals, issuance, archiving, and obsolescence) of all GxP documents, including Standard Operating Procedures (SOPs), Master Batch Records (MBRs), specifications, validation protocols, and logbooks.
• Serve as the site gatekeeper for Data Integrity, ensuring strict adherence to 21 CFR Part 11 and ALCOA++ principles across all paper-based records, hybrid records, and automated electronic system outputs.

5. Maintains expertise in various regulations and provides compliance leadership to the manufacturing site.

• Provides direct interface with FDA and other regulatory agencies and customers during inspections.
• Performs assessments to determine compliance to processes and regulations to identify potential gaps and mitigate and implement improvements within QMS.
• Establish programs to promote quality awareness and compliance.

Requirements & Qualifications

• Education: Bachelor’s degree (B.S.) in Chemistry, Pharmacy, Chemical Engineering, Statistics, or a related scientific discipline. Advanced degree is preferred.
• Minimum of 6+ years of progressive QA/QMS experience in quality assurance, quality oversight or relevant experience.
• Technical knowledge in as many of the following areas as possible: quality, regulatory, process sciences, manufacturing operations.
• Knowledge and familiarity with products, processes, equipment and facilities of pharmaceutical related products.
• Knowledge of QA systems and GMP compliance requirements including regulations and standards affecting pharmaceutical products.
• Leadership: Proven ability to manage cross-functional projects and lead technical teams through complex problem-solving. Can lead projects to deliver tactical results that support strategic initiatives.
• Communication: Excellent written and verbal communication skills, with the ability to present technical compliance data clearly to regulatory inspectors and corporate executives.
• Analytical Mindset: High attention to detail with sharp critical-thinking and risk-based decision-making skills.
• Manage and prioritize workloads and projects to ensure effective and efficient completion of departmental objectives. Experience working in both a team setting and independently. Work well with manager guidance while able to manage own time.
• Proven track record of actively defending OSD investigations, SPC charts, batch release data, training records, and document control history during successful US FDA cGMP field inspections.
• High proficiency with Microsoft Office, statistical software, and automated eQMS platforms (e.g., TrackWise, Veeva Vault, MasterControl), and SAP.

Physical Requirements

• Frequent walking, standing, and moving across the manufacturing floor to monitor operations.
• Fine motor skills required to operate computers, handle paper documentation, and inspection tools
• Ability to lift and carry up to 25 pounds.
• Ability to wear PPE/gowning for extended periods of time