Junior Associate – Quality Assurance (IPQA)
Function: Quality Assurance
Location: Bengaluru
Job Type: Full-Time
Minimum Experience: 2+ years
Posted On: May 27, 2026
Experience Level
2+ years of experience in Quality Assurance / In-Process Quality Assurance (IPQA)
Suitable for:
QA Officer
IPQA Executive
Production QA support roles in pharmaceutical manufacturing
Salary
Estimated market salary: ₹3.5–6.5 LPA CTC (can go up to ₹7–8 LPA in larger pharma companies or sterile/regulated manufacturing setups).
Role Summary
The Junior Associate – Quality Assurance is responsible for ensuring in-process quality compliance in pharmaceutical manufacturing. The role focuses on line clearance, batch record verification, in-process checks, documentation review, and ensuring adherence to GMP standards throughout manufacturing and packaging operations.
Key Responsibilities
In-Process Quality Assurance (IPQA)
Perform line clearance before manufacturing and packaging stages.
Verify raw materials and process orders against batch records.
Ensure compliance with GMP during production activities.
Monitor in-process manufacturing and packaging operations.
Batch Manufacturing Record (BMR) Control
Issue, verify, and maintain batch manufacturing and packing records.
Ensure correct version control of batch records.
Archive master copies and manage documentation lifecycle.
Maintain batch record issuance registers.
Material & Process Verification
Cross-check raw materials and packaging materials during dispensing.
Verify intermediate and finished goods against specifications.
Ensure correct material usage as per process orders.
Sampling & Testing Support
Collect and submit samples:
Process validation samples
Stability samples
Control samples
Analytical samples
Quality Checks & Calibration
Conduct in-process testing (physical parameters, as per BMR).
Support periodic calibration of instruments such as:
Friabilator
Disintegration tester
pH meter
Weighing balances
Documentation & Compliance
Review completed batch records.
Verify production logbooks and calibration records.
Ensure compliance with SOPs and GMP guidelines.
Prepare Annual Product Quality Review (APQR).
Audit & Quality Systems
Support internal and regulatory audits.
Assist in change control documentation.
Ensure proper documentation practices across production areas.
Required Skills & Knowledge
Knowledge of GMP (Good Manufacturing Practices)
Understanding of pharmaceutical manufacturing processes
IPQA experience in solid oral dosage or sterile manufacturing preferred
Strong attention to detail
Documentation and regulatory compliance skills
Basic understanding of QC/QA systems
Familiarity with batch records and SOPs
Key Competencies
Quality Assurance (IPQA)
GMP Compliance
Batch Record Review
Line Clearance Activities
Sampling Techniques
Documentation Control
Instrument Calibration Support
Regulatory Awareness
Ideal Candidate
A pharmaceutical QA professional with hands-on manufacturing floor experience, strong understanding of GMP compliance, and exposure to batch record handling, in-process checks, and documentation control in a regulated production environment.
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