Aizant Drug Research Solutions Pvt. Ltd is an integrated drug development solutions provider. Aizant was established by experienced pharmaceutical professionals with global exposure. We are a rapidly growing formulation CDMO and CRO with a diverse portfolio of capabilities partnering with health care companies specializing in new molecular entities (NMEs), generics (ANDA’s) and over the counter (OTC’s) products globally.
We are conducting walk-in interviews for following..!!!
- Department: Quality Control
- Role:- Stability/ RMPM / AMV / IPFP
- Designation: Executive / Sr. Executive
- Location: Hyderabad
Job description:
- Preparation of Record of analysis (ROA)
- Loading, withdrawal, testing and review of stability samples
- To sample receive, analyze and review of In-process, Finished products and Stability samples
- Daily temperature and humidity monitoring and review of Stability chambers, Reserve/ Reference sample room and QC instrumentation lab
- Receiving of specifications, STPs, log books and SOPs from QA
- Ensuring the compliance w.r.t Good laboratory practice (GLP)
- To ensure that the HPLC/ GC columns are used and maintained properly as per GLP
- To sample, analyze and review of Raw materials and Packaging materials.
- To coordinate with supervisor in developing the methods for dissolution, assay by UV/ HPLC and RS by HPLC.
- Preparation of validation protocols, validation report.
- Perform validation of test procedures like Dissolution, Assay, Related substances, Residue, water content, identifications and Chiral purity etc.,
Date: 9th September, 2022
Time: 9.30 AM – 12.00 PM
Venue: Aizant Drug Research Solutions P Ltd, Sy No. 172 & 173, Apparel Park Road, Dulapally,
Quthbullapur Mandal, Hyderabad, Telangana – 500 100
