Aizant 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 (ANDAs) and over the counter (OTCs) products globally.
Post : Executive / Senior Executive
Department : QUALITY CONTROL
Experience : 2-6 years
Qualification : BSc/MSc (Chemistry), B.Pharmacy / M.Pharmacy.
Job Role : Testing/Analysis of Raw Material / ln-Process /Finished Products/Stability Samples. Method Validation/Preparation of validation protocols/Validation report
Required Skills : Hands on experience on HPLC/GC/UV Exposure in regulatory Audits. Good knowledge of CGMP, GLP and GDP.
Job 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.,
Walk-in Interview
Date & Time : 9th Sep 2022 from 9:30am to 1:00pm
Venue : Aizant Drug Research Solutions Pvt Ltd Sy. No. 172 & 173,
Quthbullapur Mandal, Apparel Park Rd, Dulapally, Hyderabad,
Telangana 500100
email : careers@aizant.com
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