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Qa Executive – Quality Assurance (Ipqa / Gmp Compliance / Documentation)

IPCA Laboratories Limited
0-3 years
Not Disclosed
Dhar, India
1 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing

QA EXECUTIVE – QUALITY ASSURANCE (IPQA / GMP COMPLIANCE / DOCUMENTATION)

JOB SUMMARY
A Quality Assurance (QA) Executive role responsible for ensuring compliance with GMP standards across manufacturing operations, in-process quality monitoring (IPQA), documentation control, and batch record review. The role ensures that pharmaceutical manufacturing processes consistently meet regulatory, internal quality, and audit requirements.

EXPERIENCE REQUIRED
Fresher to 3 years of experience in Quality Assurance, IPQA, or pharmaceutical manufacturing compliance. Freshers with strong GMP and industrial training exposure are eligible.

EDUCATION QUALIFICATION
B.Pharm (Bachelor of Pharmacy)

KEY RESPONSIBILITIES

  • Perform QA documentation activities ensuring accuracy, completeness, and compliance with GMP standards

  • Conduct In-Process Quality Assurance (IPQA) checks during manufacturing operations

  • Ensure adherence to GMP guidelines, SOPs, and regulatory compliance requirements

  • Review batch manufacturing records (BMR) and batch packaging records (BPR) for accuracy and completeness

  • Support validation activities including process validation and cleaning validation documentation

  • Coordinate with Production and Quality Control teams to ensure quality compliance at all stages

  • Participate in internal audits, GMP audits, and regulatory inspections

  • Identify deviations and support investigation and CAPA implementation

  • Ensure proper documentation control and maintenance of quality records

KEY SKILLS REQUIRED

  • Strong understanding of GMP, GDP, and pharmaceutical quality systems

  • Knowledge of IPQA processes and in-process manufacturing controls

  • Experience in audit handling and documentation review

  • Strong attention to detail and compliance mindset

  • Good communication and coordination skills across cross-functional teams

  • Ability to work in a regulated manufacturing environment