Bhakti Dixit

QA Documentation and IPQA professional with 1 year of pharmaceutical industry experience in GMP-compliant manufacturing environments. Experienced in QA documentation, BMR/BPR review, document issuance and retrieval, line clearance, IPQA monitoring, process validation, stability studies and audit support. Familiar with SOP compliance, production and packing activities, and quality system documentation.

QA Officer - Medico Remedies Ltd. - Palghar

(2025-05)

• Preparation of APQR, PVP, PVR, Stability Study Protocol and Hold Time Study Protocol.
• Document issuance and retrieval as per QA documentation requirements.
• Review of BMR and BPR during production and packing stages.
• Performed line clearance during dispensing, manufacturing and packing.
• Daily monitoring of production and packing activities as part of IPQA.
• Performed process validation activities and withdrew validation samples as per protocol.
• Withdrawal of registration, stability, control and reference samples.
• Maintained IPQC logbook and ensured SOP compliance.
• Supported audits including WHO and customer/party audits.

Pharmacist - Truemeds E-Pharmacy - Andheri

(2024-07 - 2025-04)

Bachelor of Pharmacy - Pharmacy (2024)