Metrochem Walk-in On 29th May to 6th Jun 2026 Freshers & experience

Review batch manufacturing, packing, cleaning, and equipment logbook documents for completeness, accuracy, signatures, and compliance with approved procedures.

Monitor shopfloor operations to ensure adherence to GMP practices, SOP compliance, hygiene standards, and data integrity requirements.

Issue, control, reconcile, and archive GMP documents including batch records, logbooks, labels, formats, and annexures as per document control procedures.

Perform in-process checks and operational verification activities during manufacturing and packing to ensure process compliance and procedural adherence.

Support deviation, incident, CAPA, change control, and investigation activities through preliminary data collection, documentation support, and follow-up coordination.

Coordinate sample collection and submission activities for analysis, retention, and stability studies as per approved quality procedures.

Ensure compliance with Good Documentation Practices (GDP) including proper entries, corrections, contemporaneous recording, and documentation traceability.

Participate in GMP walkthroughs, internal audits, and audit readiness activities through document retrieval, compliance verification, and observation closure support.

Coordinate with Production, QC, Warehouse, and Engineering departments for execution of quality assurance activities and compliance with GMP, EHS, and regulatory requirements.

This is a walk-in post. Even then candidates are encouraged to share their resumes in advance at talenthire-unitb@metroapi.com with the subject line Profile for QA This will help our team connect with you beforehand and guide you about the position. We warmly welcome candidates who are currently working in Hyderabad and nearby areas and who wants to start their professional career in QA department.