Job Description
The person should be skilled in using Labware and able to prepare, review and approve RBE masters in LIMS.
Should have skilled in preparation of Specification and STPs through LAbware LIMS application,
Should manage stock preparation and inventory, including chemicals, standards and columns in LIMS.
Need to handle master records and requirements, address issues and support solutions in LIMS.
Must maintain analyst qualification records and instrument registration in LIMS.
Should identify training needs and ensure the department completes training on time.
Responsible for investigating incidents, out-of-specifications (OOS) and out-of-trend (OOT) issues and ensuring timely resolution.




Need to handle change control and CAPA (Corrective and Preventive Actions) related to the quality control department, ensuring timely resolution and effectiveness checks.
Must ensure all changes to specifications, STPs (Standard Test Procedures), and SOPs (Standard Operating Procedures) are evaluated and communicated effectively.
Should periodically review and spot-check specifications and STPs in use.
Need to compile data related to Quality Risk Management (QRM).
Need to perform instrument interface activity and user able to perform SAT and UAT
⁠B.Pharm/M.:Pharm/M.Sc

📌 Team Member Lims Pydibimavaram
🏢 Dr. Reddy's Laboratories
📍 Pydibimavaram