Hardik P.
Mid-Level Pharmaceutical Quality Assurance Officer
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Hardik R. is a skilled Quality Assurance Officer boasting 4 years of experience in the pharmaceutical industry. With expertise in QMS documentation, SOP preparation, Change Control, CAPA, and GMP Compliance, he has vastly contributed to quality systems and regulatory compliance in his roles. At BDR Pharmaceuticals International Pvt. Ltd. from June 2022 to June 2025, Hardik was responsible for preparing and reviewing standard operating procedures, batch records, and managing document control through SAP software. Since June 2025, at Pharma Inter Chemie (API), Hardik has continued to significantly contribute by coordinating with various departments to ensure stringent compliance activities. His academic background includes a B.Sc and an ongoing M.Sc in Chemistry, lending further technical depth to his capabilities in the field.
Experience
QA-OFFICER
BDR PHARMACEUTICALS INTERNATIONAL PVT. LTD. · 2022 — 2025Conducted the preparation and review of SOPs, Batch Records, and Daily Logbook Records. Managed the effective review and issuance of controlled copies of SOPs, specifications, and standard test procedures. Utilized SAP software for the issuance of BMR/BPR. Maintained the SOP index and communicated with relevant departments for SOP re-reviews. Handled the cancellation, superseding, and obsolescence of master documents according to change control protocols. Ensured stock management of perforated worksheets and registers and raised purchase requests through SAP software. Took responsibility for the preparation and review of additional quality-related documentation. Issued change control documents and managed tasks involving SAP, ICDAS, and SCADA software.QA-OFFICER
PHARMA INTER CHEMIE (API) · 2025 — PresentOversaw the preparation, review, and control of SOPs, formats, and records. Issued documentation related to the Quality Management System (QMS) and managed the issuance, retrieval, and archival of controlled documents and logbooks. Provided documentation support for change control, CAPA, and document control activities. Managed documentation related to deviations and CAPA records. Coordinated training and maintained records within the documentation system. Prepared and reviewed Annual Product Quality Review (APQR) reports while collaborating with the QC, warehouse, production, and other departments for compliance documentation and activities.
Skills & Expertise
Education
- M.Sc ChemistrySGGU University · — — 2026
- B.Sc ChemistrySGGU University · — — 2022
- H.S.CG.HS.E. B Board · — — 2013
- S.S.CG.S.E.B Board · — — 2011
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