Walk In Interview at Intas SEZ For ( IPQA - OSD and Injectable )
Intas · Ahmedabad
- Experience2–6 yrs
- SalaryNot disclosed
- Work modeonsite
- Posted26 Sept 2026
About Intas
Intas is hiring in Ahmedabad in pharma biotech. This role looks for around 2+ years of experience.
Skills
- cGMP
- Good Documentation Practices
- OSD manufacturing
- Batch Manufacturing Records
- Batch Packing Records
- WHO-GMP
- EU-GMP
- USFDA
- MHRA
- Microsoft Office
- Data Integrity
- CAPA
- Change control
- Risk assessment
The role
An IPQA officer at a pharmaceutical manufacturing company performs cGMP compliance, OSD manufacturing quality checks, and regulatory audits while applying Good Documentation Practices and Batch Manufacturing Records.
Full job description
Job Purpose
To ensure compliance with cGMP requirements during the manufacturing and packing of Oral Solid Dosage (OSD) and Sterilize injectable products through line clearance, in-process checks, documentation review, and monitoring of manufacturing activities.
Key Responsibilities
Production Area Monitoring
Perform line clearance before the start-up of manufacturing and packing activities.
Monitor dispensing, granulation, blending, compression, coating, capsule filling, and packing operations.
Ensure adherence to approved Batch Manufacturing Records (BMR) and SOPs.
Verify equipment status labels and cleanliness before use.
In-Process Quality Checks
Conduct and record in-process checks as per approved specifications and frequencies.
Monitor critical process parameters during manufacturing.
Verify weight variation, hardness, thickness, friability, disintegration, and visual inspection results.
Ensure proper sampling during various manufacturing stages.
Documentation & Compliance
Review BMR/BPR entries for completeness and accuracy.
Ensure Good Documentation Practices (GDP) are followed.
Monitor adherence to cGMP, Data Integrity, and regulatory requirements.
Issue, control, and reconcile manufacturing-related documents.
Line Clearance & Area Control
Conduct area and equipment line clearance before and after batch processing.
Verify removal of previous product materials and documents.
Ensure proper status labeling and segregation of materials.
Quality Systems
Participate in investigations related to deviations, incidents, OOS, and customer complaints.
Support CAPA implementation and effectiveness verification.
Assist in change control and risk assessment activities.
Support internal, customer, and regulatory audits.
Sampling Activities
Perform in-process, hold-time, and finished product sampling as per approved procedures.
Coordinate with the QC department for sample testing and release activities.
Training & Continuous Improvement
Provide GMP awareness and compliance support to production personnel.
Participate in quality improvement initiatives.
Support implementation of quality culture across manufacturing operations.
Qualifications
Education
B.Pharm / M.Pharm
Officer to Executive: 2-6 years of experience in IPQA activities within a pharmaceutical manufacturing facility.
Required Skills
Knowledge of cGMP, GDP, and regulatory requirements.
Experience with OSD manufacturing processes.
Strong documentation and investigation skills.
Knowledge of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR).
Familiarity with regulatory standards such as WHO-GMP, EU-GMP, USFDA, and MHRA.
Good communication and coordination skills.
Proficiency in MS Office.
Key Competencies
Attention to detail
Analytical thinking
Problem-solving ability
Quality mindset
Team collaboration
Regulatory compliance focus
Preferred Industry: Pharmaceutical