Quality Assurance Job at Syngene for Pharmacology Graduates – Apply Now!
Are you a postgraduate in Pharmacology passionate about quality and regulatory standards? Syngene International Ltd. is hiring for a GLP Quality Assurance role at its cutting-edge facility in Bangalore. If you have experience with OECD GLP, ICH, or WHO-GCLP, this is your opportunity to work in a globally respected CRO and contribute to world-class bioanalytical research.
About Syngene:
Syngene is a global innovation-driven contract research, development, and manufacturing organization. With integrated scientific services ranging from early discovery to commercial supply, Syngene offers a collaborative, safety-first, and compliance-focused work environment.
- Job Title: GLP QA Personnel
- Location: Bangalore, India
- Employment Type: Full-Time
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Ensure adherence to OECD GLP, ICH, and WHO-GCLP guidelines
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Manage QMS processes including change controls, deviations, and CAPA
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Review and audit SOPs, study plans, MOAs, and reports
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Conduct study-based, facility-based, and process-based inspections
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Audit PK and ADA study raw data and final reports for large molecules
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Review computerized systems for compliance with OECD Principle 17 and 21 CFR Part 11
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Participate in internal and external inspections or audits
Eligibility Criteria for Quality Assurance Job:
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Master’s degree in Pharmacology or any relevant discipline
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Prior experience in GLP labs with strong knowledge of regulatory compliance
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Skilled in SOP review, documentation audits, and handling complex QMS activities
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Good scientific reasoning, communication, and collaboration skills
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Ability to work on multiple software platforms and manage documentation workflows
What Syngene Offers:
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Exposure to global standards in GLP, GCLP, and bioanalytical studies
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Career growth in a high-impact regulatory and QA environment
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Training, safety-first culture, and a collaborative team ecosystem
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Opportunity to contribute to impactful scientific research
