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Pharma IPQA Jr. Chemist

Job Title: Junior Chemist IPQA (In-Process Quality Assurance)

Department: Quality Assurance

Experience: 02 years / Freshers can be considered

Qualification: B.Sc./M.Sc. Chemistry, B.Pharm/M.Pharm, or related pharmaceutical/life-science qualification, depending on the organization.

Job Summary

Responsible for performing in-process quality assurance activities on the pharmaceutical manufacturing shop floor and ensuring that manufacturing and packaging operations comply with approved SOPs, GMP, GDP, specifications, and batch records . Typical IPQA chemist roles include quality checks, identification/reporting of non-conformities, documentation compliance, and data integrity.

Key Responsibilities

- Perform line clearance for dispensing, manufacturing and packing areas.
- Conduct in-process checks during manufacturing and packaging.
- Monitor critical process parameters and verify compliance with approved procedures.
- Perform sampling of raw materials, in-process materials, finished products and other samples as per SOP/protocol.
- Review BMR/BPR and associated production documents for completeness and accuracy.
- Check equipment, area, cleaning, calibration and housekeeping records.
- Ensure compliance with GMP, GDP and data-integrity requirements .
- Identify and immediately report deviations, non-conformances and abnormal observations.
- Assist in deviation, CAPA, change-control and investigation activities.
- Verify batch reconciliation, yield and material usage.
- Perform routine GMP/shop-floor inspections.
- Coordinate with Production, QC, Warehouse and Engineering for quality-related activities.




- Maintain IPQA checklists, logbooks and daily reports.
- Support qualification and validation activities such as process validation and cleaning validation , where applicable.
- Assist during internal audits and regulatory inspections.
- Follow EHS requirements and maintain proper PPE and housekeeping practices. Required Knowledge & Skills

- Basic knowledge of Pharmaceutical GMP and GLP
- Good Documentation Practices ( GDP )
- Knowledge of BMR/BPR and SOPs
- Basic understanding of deviations, CAPA and change control

- Sampling and in-process inspection techniques
- Attention to detail and positive observation skills

- Basic computer/MS Office skills

- Good communication and teamwork

- Willingness to work in shifts and on the manufacturing shop floor

Key Performance Areas

- Accurate and timely IPQA checks

- Proper line clearance

- Real-time documentation

- GMP compliance

- Accurate BMR/BPR review
- Timely reporting of deviations/non-conformities

- Audit readiness

- Data integrity and documentation accuracy

For a fresher , the role is generally more focused on shop-floor monitoring, line clearance, sampling, documentation and learning GMP/IPQA systems rather than independently handling complex investigations.

If you mean JD for Pharma IPQA Jr. Chemist for resume/job application , I can also give you a short HR-style JD with required skills and interview questions .

Disclaimer: This job posting and Location has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.

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