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Janaki Pharma

Janaki Pharma

Pharmaceutical Quality Assurance Officer

Talent
WatfordMember since August 26, 2026
GMPGDPGxP ComplianceBatch Manufacturing Record (BMR) / Batch Packaging Record (BPR) ReviewDeviation Documentation, Investigation Support & CAPA TrackingChange Control & Controlled Document ManagementSOP Compliance, Audit Preparation & Inspection ReadinessData Integrity (ALCOA+) & Quality Record ArchivingHygiene Control, Contamination Prevention & Health and SafetyCross-Functional Collaboration with Production & QC TeamsMicrosoft Office (Word, Excel, Outlook)
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GMPGDPGxP ComplianceBatch Manufacturing Record (BMR) / Batch Packaging Record (BPR) ReviewDeviation Documentation, Investigation Support & CAPA Tracking

About

Pharmaceutical Quality Assurance professional and pharmacy graduate (B.Pharm) with hands-on experience supporting GMP/GDP-compliant documentation, batch manufacturing and packaging record (BMR/BPR) review, deviation investigation, CAPA tracking, controlled document management, and audit readiness within a regulated pharmaceutical manufacturing environment. Complements this with recent UK-based experience in high-care, hygiene-controlled production and care settings, applying strict contamination control, PPE, health and safety, and standard operating procedure (SOP) compliance. Seeking to bring strong attention to detail, data integrity awareness, and cross-functional collaboration skills to a Quality Assurance Officer, QA Associate, QA Compliance, or Document Control role in the UK pharmaceutical or life sciences sector.

Experience

QA Officer - Bhumi Pharmaceuticals - Vadodara, India

(2021-11 - 2023-12)

  • Reviewed batch manufacturing and packaging records for completeness, accuracy, traceability, and compliance with approved SOPs and current GMP requirements.
  • Maintained controlled quality documentation including SOPs, logbooks, batch records, quality records, registers, and archival files in line with data integrity principles.
  • Identified, documented, and supported investigation follow-up and closure of deviations and quality-system events.
  • Tracked CAPA actions and followed up with cross-functional teams to ensure timely completion of corrective and preventive measures.
  • Assisted with internal audit preparation and inspection-readiness activities, liaising with Production and QC teams to resolve documentation discrepancies.
  • Supported accurate, legible, contemporaneous, and controlled record-keeping in accordance with ALCOA+ data integrity principles.

High Care Process Operative - Elis - Fakenham, United Kingdom

(2025-03 - 2025-11)

  • Worked within a high-care, hygiene-controlled production environment, following strict cleanliness, contamination-control, PPE, hand-hygiene, and segregation procedures.
  • Processed garments and linens in accordance with site quality procedures, production targets, and health and safety standards.
  • Carried out routine operational checks and promptly reported quality, hygiene, equipment, and safety concerns.

Care Assistant - Taylor Care - Fakenham, United Kingdom

(2025-05 - 2025-11)

  • Delivered person-centred personal care in line with individual care plans, maintaining accurate, timely, and confidential care records.
  • Followed infection-control, hygiene, safeguarding, health and safety, and workplace procedures at all times.

Education

Bachelor of Pharmacy - Pharmacy - Gujarat Technological University (2016 - 2020)

Skills

Pharmaceutical Quality Assurance Officer

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