Quality Assurance Job Opening at Syngene for Life Science Graduates – Apply Now!

• Ensure adherence to OECD GLP, ICH, and WHO-GCLP guidelines

• Manage QMS processes including change controls, deviations, and CAPA

• Review and audit SOPs, study plans, MOAs, and reports

• Conduct study-based, facility-based, and process-based inspections

• Audit PK and ADA study raw data and final reports for large molecules

• Review computerized systems for compliance with OECD Principle 17 and 21 CFR Part 11

• Participate in internal and external inspections or audits

Eligibility Criteria for Quality Assurance Job:

• Master’s degree in Life Science or any relevant  discipline

• Prior experience in GLP labs with strong knowledge of regulatory compliance

• Skilled in SOP review, documentation audits, and handling complex QMS activities

• Good scientific reasoning, communication, and collaboration skills

• Ability to work on multiple software platforms and manage documentation workflows

What Syngene Offers:

• Exposure to global standards in GLP, GCLP, and bioanalytical studies

• Career growth in a high-impact regulatory and QA environment

• Training, safety-first culture, and a collaborative team ecosystem

• Opportunity to contribute to impactful scientific research