Anjana P.

About Anjana P.

Self-driven and assertive Quality Professional with over 7 years in Quality Assurance, Validation Life Cycle, CAPA, Deviation Investigation, Technology Transfer, and Project Management in the Pharmaceutical and Medical Device industries. Skilled in quality compliance activity, deviations, SOP, change control, batch record and protocol review, finished and product release, cGMP document control, and other quality operational activities.

Experience

1. Documentation Specialist

   CRB

   Nov 2025 — Present · Sanford, NC, US

   Preparing, organizing, and maintaining turnover documentation packages in accordance with the project and client requirements.• Coordinating with project teams, quality control, engineering, and construction departments to gather and verify all necessary turnover documents.• Reviewing documentation for accuracy, completeness, and compliance with internal and client standards.• Tracking document submissions, approvals, and revisions through project document control systems.• Assisting in the creation and maintenance of document logs, checklists, and tracking reports for turnover packages.• Ensuring all records, drawings, and certifications are properly compiled and formatted before projecthandover.• Supporting audits and responding to client requests for documentation and records.• Collaborating with project management to ensure the timely and accurate delivery of turnover documentation.• Maintaining confidentiality and ensuring compliance with company policies and data managementstandards.

Education

• Gayatri Vidya Parishad College of Engineering (Autonomous)

  Bachelor of Technology, Chemical Engineering

• Cleveland State University

  Masters of Science, Environmental/Environmental Health Engineering