Career Opportunity: IPQA Trainee
Hetero Plasma Sciences Ltd. is actively inviting applications from enthusiastic fresh graduates for the role of In-Process Quality Assurance (IPQA) Trainee. This opportunity is ideal for individuals passionate about initiating a career in the pharmaceutical and biopharmaceutical manufacturing industry, specifically within a robust Quality Assurance department.
This trainee position is located at Hetero Plasma Sciences Ltd. in Kothur, Telangana, and is open to freshers eager to gain practical experience within this vital industry sector.
Eligibility:
- Education: B.Pharm, M.Pharm, or M.Sc in Chemistry.
- Experience: Fresh Graduates.
Key Responsibilities will involve:
Trainees will play a crucial role in ensuring adherence to Good Manufacturing Practices (GMP) and quality standards throughout the manufacturing lifecycle. Core duties include performing and monitoring in-process quality assurance activities and conducting thorough line clearance procedures across manufacturing, warehouse, and packing operations.
A significant part of the role involves reviewing essential GMP documentation such as Batch Manufacturing Records (BMR) and Batch Packing Records (BPR). Trainees will monitor cleanroom behavior and aseptic practices, ensuring continuous compliance. They will also support manufacturing operation inspections, monitor in-process samples, and actively assist in broader quality assurance tasks.
Furthermore, responsibilities extend to participating in Process Validation, Cleaning Validation, and Annual Product Quality Review (APQR) activities. Trainees will conduct Acceptable Quality Level (AQL) inspections in the packing department and assist with Warehouse and Quality Control (QC) Plasma testing. Supporting plasma inward verification, sampling procedures, issuance activities, and associated documentation, along with maintaining comprehensive IPQA documentation and archival records, are also integral to the position.
This role offers an exceptional chance to launch a career, acquire hands-on experience within a GMP-compliant environment, and collaborate with industry experts.
