Analyst, Quality Control

Par Formulations

Full time Business Operations Specialists
Apply Now
Location
Pudupakkam, Tamil Nadu, India
Posted
July 04, 2026

Job Description

Description

  • Perform routine and stability sample analysis as per approved specifications and test methods
  • Operate and maintain analytical instruments (HPLC, GC, UV, Dissolution Apparatus, etc.)
  • Review and document analytical data in compliance with cGMP and data integrity principles
  • Investigate OOS/OOT results and support deviation and CAPA activities
  • Ensure compliance with FDA, cGMP, and GLP requirements
  • Prepare and review analytical reports, protocols, and SOPs
  • Participate in method transfer, verification, and validation activities
  • Support regulatory and internal audits
  • Strong knowledge of FDA regulations, cGMP, and data integrity
  • Analytical troubleshooting and problem-solving skills
  • Documentation and compliance expertise
  • Team collaboration and communication

    • Job Details

    • Job Type
      Full time
    • Category
      Business Operations Specialists
    • Date Posted
      July 04, 2026
    • Application Deadline
      August 13, 2026