Ramna Ramna

Dedicated and detail-oriented Quality Assurance Executive with 4 years of experience in the pharmaceutical industry. Skilled in ensuring compliance with GMP guidelines, maintaining quality documentation, handling deviations, and supporting continuous quality improvement. Seeking to contribute to organizational excellence and regulatory compliance through effective quality management practices.

Quality Assurance Executive at Velite Pharmaceuticals Pvt. Ltd. (2024-01 – Present)

• Ensured compliance with SOPs and GMP requirements.
• Investigated deviations and implemented corrective and preventive actions (CAPA).
• Managed change controls and documentation activities.
• Maintain and control QA documentation.
• Assisting in investigation and root cause analysis of quality issues.
• Participated in self inspection and internal audits.
• Handling documents revision, version control and periodic review of SOPS.
• Preparation, review, issuance and retrieval of controlled documents such as SOPs, BMR, BPR, specifications and formats.
• Issuance and reconciliation of log books and controlled copies.
• Coordination with quality control, production and other departments for documents related activities.
• Review stability protocols and reports.
• Maintaining proper retrieval records as per retention policies.
• Cordinating and monitoring stability studies as per ICH guidelines and approved protocols.
• Ensure timely withdrawal and submission of stability samples for analysis.
• Maintain stability study, ecord sample inventories and documentation.
• Monitoring storage condition of stability chamber and review temperature and relative humidity records.
• Maintaining archival and retrieval of stability protocols and reports and raw data.
• Preparation, maintaining and review of annual product quality review documentation.

Quality Assurance Officer at Cosmas Research lab Pvt. Ltd. (2021-08 – 2024-02)

• Reviewing and approving packaging artwork, label, carton, leaflets and foil materials to ensure compliance with regulatory and company requirements.
• Coordinating with regulatory affairs, production, packaging development and marketing department for artwork creation and approval.
• Maintain artwork archive and ensuring proper documents retention.
• Performing review, revision and retrieval of controlled documents.
• Cordinating and monitoring stability studies as per ICH guidelines and approved protocols.
• Ensure timely withdrawal and submission of stability samples for analysis.
• Maintain stability study, ecord sample inventories and documentation.
• Monitoring storage condition of stability chamber and review temperature and relative humidity records.
• Maintaining archival and retrieval of stability protocols and reports and raw data.
• Assisting in internal audits and regulatory inspection by providing required documents stability records and artwork records.

Quality assurance manager at Prispag pharma (2026-08 – Present)

• Reviewing and approving packaging artwork, label, carton, leaflets and foil materials to ensure compliance with regulatory and company requirements.
• Coordinating with regulatory affairs, production, packaging development and marketing department for artwork creation and approval.
• Maintain artwork archive and ensuring proper documents retention.
• Performing review, revision and retrieval of controlled documents.
• Cordinating and monitoring stability studies as per ICH guidelines and approved protocols.
• Ensure timely withdrawal and submission of stability samples for analysis.
• Maintain stability study, ecord sample inventories and documentation.
• Monitoring storage condition of stability chamber and review temperature and relative humidity records.
• Maintaining archival and retrieval of stability protocols and reports and raw data.
• Assisting in internal audits and regulatory inspection by providing required documents stability records and artwork records.
• Ensured compliance with SOPs and GMP requirements.
• Investigated deviations and implemented corrective and preventive actions (CAPA).
• Managed change controls and documentation activities.
• Maintain and control QA documentation.
• Assisting in investigation and root cause analysis of quality issues.
• Participated in self inspection and internal audits.
• Handling documents revision, version control and periodic review of SOPS.

Bachelor of pharmacy in Pharmacy – CT University (2017 – 2021)

Senior secondary – Swami Roop Chand Jain senior secondary public school (2016)

Matriculation – Swami Roop Chand Jain senior secondary public school (2014)