Experience in Oral Solid Dosage Manufacturing / CVC Packaging. Exposure to the latest manufacturing and packing techniques. Familiar with cGMP guidelines and Quality Systems as per the international regulatory requirements
B.Sc, M.Sc, B. Pharm with 3-7 years of experience in handling of all raw material dispensing operations. Candidates should be well versed with SAP WMS, QMS, Qualification and MES, Automated Dispensing System and should have exposure to USFDA, MHRA and other regulatory audits.
Analysis of Raw material, Stability and Finished product samples, must have hands on experience of instruments like, HPLC, GC, UV, KF, ICPMS & IR etc., QC investigation and QMS.
Experience in analysis of FP, IP, PV and stability’ samples and method validation and method transfer. Experience of handling of various instruments and expertise in Chromatography and Spectroscopy analysis.
Execute strategic business plans tailored to augment our footprint in the Formulation segments, in alignment with organizational objectives. Forge and nurture robust relationships with key clients, distributors, and stakeholders to fortify business alliances and cultivate enduring partnerships.
Driving sales to achieve targets and ensuring a healthy P&L for the regional countries. Liaising with clients to ensure optimum inventory levels are maintained to ensure optimum sales are achieved
M.Pharma, M.Sc in Life Sciences. National Network Component. Development of antimicrobial peptide tagge nanoformulation for targeted combination therapy against Pseudomonas aeruginosa.
Ab initio insights into the molecular level mechanism of sorption enhanced steam methane reforming on hybrid materials. Design and development of vapor phase catalytic ammoxidation for conversion of dilute bioethanol to acetonitrile