About this role
About the Role Dr. Reddy’s Laboratories seeks a LIMS/Labware specialist to support QC operations by preparing, reviewing and approving LIMS/RBE master data, managing stock and master records, and maintaining qualification/instrument registration in LIMS. The role includes handling training, incident investigations, change control, CAPA, specifications updates, QRM data compilation and instrument interface activities, with participation in SAT and UAT. What You'll Do
- Use Labware and prepare, review and approve RBE masters in LIMS
- Manage stock preparation and inventory (chemicals, standards, columns) in LIMS
- Handle master records and requirements; address issues and support LIMS solutions
- Maintain analyst qualification records and instrument registration in LIMS
- Identify training needs and ensure on-time department training
- Investigate incidents, OOS and OOT issues and ensure timely resolution
- Manage change control and CAPA related to the QC department, ensuring timely resolution and effectiveness checks
- Ensure all changes to specifications, STPs and SOPs are evaluated and communicated
- Periodically review and spot-check specifications and STPs in use
- Compile data related to Quality Risk Management (QRM)
- Perform instrument interface activity and be able to conduct SAT and UAT What We're Looking For
- B.Pharm/M.Pharm or Pharm/M.Sc
- Good exposure to LIMS and MS Office
- Experience with Labware/LIMS preferred Compensation & Benefits
- Benefits include joining & relocation support, family support (maternity & paternity), learning and development opportunities
- Medical coverage for self and family, life insurance for the employee
- Other standard industry benefits and a focus on career development