Syngene
Incorporated in 1993. Syngene is an internationally reputed custom research and manufacturing organization, which supports R&D programs from lead generation to clinical supplies. Our multi-disciplinary skills in integrated drug discovery and development include capabilities in medicinal chemistry, biology, in vivo pharmacology, toxicology, custom synthesis, process R&D, cGMP manufacturing, formulation and analytical development along with Clinical development services.
Our highly experienced scientific and project management teams ensure:
- Timely execution of projects
- Cost effectiveness and quality of the projects
- Confidentiality and protection of intellectual property
Job Title: Lead QA – Material management Formulations
No. of Posts: 1
Job Description:
- Review of SOPs, line clearance documents for dispensing activities and material receipt documents.
- Review of vendor qualification for API, excipient and packing material suppliers.
- Periodic review and updation of approved vendor list.
- Assessment of change controls, deviations and risk assessment for warehouse activities.
- Finished goods dispatch clearance and verification.
