Validation · IPQA · Whitefield, Bangalore

Validation & IPQA

Coordinate, execute, review, and maintain validation, qualification, and IPQA activities for facilities, equipment, utilities, and processes in compliance with GMP requirements.

Validation · IPQA · Whitefield, Bangalore
Full-Time
GMP Compliance
Quality Assurance

Summary / Overview

  • Responsible for coordinating, executing, reviewing, and maintaining validation and qualification activities for facilities, equipment, utilities, processes in compliance with GMP requirements.
  • Responsible for handling of IPQA activities.

Key Responsibilities

  • Preparation and review of equipment and utility qualification protocols, reports, and supporting documents, including HVAC, water systems, compressed air, and chillers.
  • Ensure validation documentation complies with GMP, EU GMP, WHO GMP, Schedule M, and applicable regulatory requirements.
  • Maintain validation protocols, reports, schedules, and qualification records.
  • Coordinate temperature/humidity mapping, differential pressure verification, and other facility qualification activities.
  • Prepare and review process validation protocols and reports.
  • Establish and maintain periodic requalification schedules.
  • Conduct validation-related risk assessments.
  • Perform line clearance and in-process checks in manufacturing and packing activities.
  • Review BMRs, BPRs, logbooks, checklists, and other manufacturing records for completeness and compliance.
  • Identify and document process deviations.
  • Coordinate and perform sampling of in-process, finished products, and validation samples as per approved procedures.
  • Review IPQA-related documentation and ensure all required checks are completed before batch release.

Skills and Competencies

  • Strong knowledge of GMP, EU GMP, WHO GMP, Schedule M, and applicable regulatory requirements.
  • Good understanding of the qualification lifecycle, including DQ, IQ, OQ, PQ, and equipment qualification principles.
  • Ability to prepare, review, and execute validation protocols, reports, risk assessments, and qualification documents.
  • Good knowledge of change control, deviation, CAPA, and risk assessment.
  • Good communication and teamwork.
Job Details
LocationWhitefield, Bangalore
Employment TypeFull-Time
ExperienceNot Specified
DepartmentValidation / IPQA
PostedAugust 2026
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