Skip to main content
Dr. Reddy's Laboratories

Team Member - Quality Control

1w

Dr. Reddy's Laboratories

Baddi, IN · Full-time · INR 300,000 – INR 500,000

About this role

As a Team Member in Quality Control, perform analysis of raw materials (RM) and packing materials (PM) as per approved specifications and SOPs. Operate, troubleshoot, and routinely use HPLC and GC systems with Empower software. This role ensures product quality in a pharmaceutical laboratory setting.

Conduct potentiometric titrations and Karl Fischer (KF) water content analysis daily. Use IR spectroscopy for material identification. Handle precise testing to meet regulatory standards in pharmaceutical manufacturing.

Review and document analytical data in LIMS software while maintaining GMP and data integrity compliance. Adhere to laboratory safety practices, SOPs, and regulatory guidelines. Work independently or collaboratively in a compliance-focused environment.

Support audits, investigations, and laboratory activities as required. Develop strong analytical and troubleshooting skills through hands-on instrument operation. Contribute to quality assurance in a dynamic pharma team.

Requirements

  • Hands-on experience in HPLC and GC analysis using Empower software
  • Experience with potentiometric titration
  • Proficiency in water determination by Karl Fischer (KF)
  • Experience with IR spectroscopy
  • LIMS software operation
  • Good understanding of GMP, SOPs, and documentation practices
  • Strong analytical, troubleshooting, and compliance mindset
  • Ability to work independently as well as in a team

Responsibilities

  • Analyze raw materials (RM) and packing materials (PM) as per approved specifications and SOPs
  • Operate, troubleshoot, and routinely use HPLC and GC systems with Empower software
  • Perform potentiometric titrations and Karl Fischer (KF) water content analysis
  • Conduct analysis using IR spectroscopy for material identification
  • Review data, document results, and ensure compliance with GMP and data integrity requirements
  • Handle, review, and document analytical data in LIMS software
  • Adhere to laboratory safety practices, SOPs, and regulatory guidelines
  • Support during audits, investigations, and laboratory activities as required