Work as IPQA Team Member at Dr.Reddy's Lab

Dr.Reddy's Laboratories offers a competitive total rewards package including base salary determined on the basis of role, experience, skill set and location. Additionally, employees are eligible for an annual discretionary bonus, and benefits including comprehensive health care coverage, retirement savings plan and leave benefits. Additional details about total compensation and benefits will be provided during the hiring process.

Post : Team Member - IPQA

Job Description
• To perform In process checks, line clearance, sampling at appropriate stages (at semi-finished and finished product), during manufacturing and packing of products for cosmetic, and dental formulation.
• To follow GMP, GDP, Data integrity & safety principle in performing the defined Role & Work.
• To participate in validation activities (Process validation, Cleaning validation and Hold time sampling and qualification activities).
• To review of BMR/ BPR and release for next step of processing.
• To ensure that the Standard Operating Procedures are followed in day to day activity.
• To ensure that the environmental conditions are monitored in respective areas of the operation as per Standard Operating Procedure.
• Verification of raw material/packaging materials during dispensing.
• Maintaining IPQA records and ensures that records are updated as per procedure.
• To collect in process, intermediate and finished sample of the product being manufactured.
• Responsible for the Handling and management of Reserve samples and stability samples.
• Monitoring the area cleanliness and sanitation in manufacturing, packing, and warehouse.
• To ensure the proper status labelling to provide easy traceability and identification of material or product.
• Preparation and data collection of Annual Product Review.
• Issuance and Archival of documents from doc cell for compliance.
• Review of archived and issued documents from doc cell for compliance. (Issuance and Archival)
• Responsible for retrieval and archival of documents and updation of log books.
• Management of document life cycle (Preparation, review, verification/ approval distribution, retrieval, withdrawal, obsolete) in DMS as per define procedures.
• Any other work assigned by Team leader and Department Head.

Additional Information
Qualification : B.Pharm
Location : Baddi, Himachal Pradesh, India
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : Quality Assurance
End Date : 30th August 2026