Walk in interview for M.Pharm, B.Pharm, M.Sc, B.Sc at Aculife Healthcare | QA, QC, F&D, R&D, Packing, Production

Aculife Healthcare Private Limited is one of world’s largest Infusion & Injectable Company, having its global operation spread across 70 countries including JV Company in Brazil & wholly owned subsidiary in Mexico. 8 Manufacturing Plants Backed up by state of the art. Aculife Research Centre & 4000 plus Employee base in India & abroad. To keep up with the scale of operations & requirements of regulated and semi regulated markets, Aculife is enhancing its focus on healthcare initiatives across the global Markets.

Research & Development Analytical development & Validation Associate: M.Pharm / B.Pharm / B.Sc / M.Sc with 3-6 yrs exp in testing and documentation of-HPLC/UV Spectroscopy,'Dissolution/GC/AAS/IC etc with expertise in Comparative dissolutlon/lmpurity profllatiorVAnalytical method Validation & VenficatiorVStabie sample anatysis/Stress Testing.

Formulation Development Associate: M.Pharm with 3-5 yrs exp In Injedable/Solid Dosage formulation & regulated market. Product Development report/Optimizatlon study protocol.1 Validation Protocol preparation & execution is mandatory.

Packing Development Officer: M.Pham / B.Pharm / B.Sc with 3-5 yrs exp & knowledge of Pharma product (Injectable/Solid) packing, understanding the pharma stability concept vs packing requirement of product

 

Quality Assurance: B.Sc / M.Sc / B.Pharm / M.Pharm with 1 to 7 yrs of relevant exp In IPQA. Validation / Qualification. QMS. etc in Parenteral / Injectable dosage forms.

Quality Control: B.Sc / M.Sc / B.Pharm / M.Pharm with 1 to 7 yrs exp in stability studies, microbial monitoring, analysis of RM. FP/1P& validation samples. Exp in handling of HPLC, GC. UV & TOC shall be preferred.

Production: (Production/Packing Chemist): B.Sc / M.Sc / B.Pharm having 1-5 yrs exp in pharma product mfg like IV fluid injection (BFS and Glass), liquid & powder Injection & Dry Syrup (preferably CEPHA-'BETA). tablet & capsule including knowledge of GMP. GDP S Regulatory audits.

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