Team Member - LIMS

• The person should be skilled in using Labware and able to prepare, review and approve RBE masters in LIMS.
• 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

Good exposure in LIMS

MS Office