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This is a non-supervisory position in the Compendial Development Laboratory within Global Laboratory Operations. The incumbent will be responsible for performing analytical method development and validations for USP, NF monographs and maintaining safety and a GLP environment in the lab. Prepare and review project plans, reports, laboratory notebooks/Laboratory Management System LMS, and compile project data as required. Masters Degree in Chemistry Analytical/Organic or Pharmaceutical Sciences

Performing medical writing tasks for trial and/or non-trial activities within clinical reporting including but not limited to preparation of Protocols, Clinical Trial Reports CTRs, Non-interventional study reports NSRs, Layperson Summary LPS, Investigator Brochure and Regulatory response documents. PhD, MSc, MPharm, PharmD

Experience in injectable plant IPQA, GLP- QA, Tech Transfer, Validation, Qualification, QMS. Preference will be given to the candidates having experience of working in sterile pharma plant. M.Pharm, B.Pharm, M.Sc

HPLC, GC, Dissolution apparatus and UV Visible Spectrometer. Should also have knowledge of weight analysis, stability studies, for Injectable dosage forms.Also require candidate with experience of Bio Assay QMS and analytical data Review. B.Pharm / M.Pharm. Supervising and Controlling Production areas like Isolator, Aseptic Filling, Vial Washing, Autoclave, Lyophilizer and Visual Inspection. Should have knowledge of QMS activities.

This position would be supporting API Sales & Marketing projects for global API business. Preparation of monthly reports, internal and external data base, and annual expense budgets. Keep abreast with key regulatory changes and market developments in designated region, country.

Lab experience for Analytical Method Development, regular and stability sample analysis. Handling of HPLC for Assay, Dissolution, Related substances tests for solid orals. Perform pre-formulation studies, R and D trials and support scale-up activities Conduct R and D trials for oral solid dosage forms tablets, capsules, etc. M.Pharm / MSc

M.Sc Life Sciences / M.Pharm; Applications are invited for the above positions having the relevant experience as GLP study director/ Study personals in reputed CRO companies. Hiring for various position in different departments at Vivo Bio Tech Ltd

Downstream and Upstream Manufacturing Mammalian and Microbial, QMS; DP Medical Device, Packing and Visual Inspection Labelling, Cartoning, Pick and Place Robotic Machines Handling and Track and Trace; DP and DS Engineering, Maintenance Automation, Instrumentation, Injectable Maintenance, QMS; M.Pharm, B.Pharm, MSc Chemistry, Biotechnology, Life science, Microbiology

GLP, Raw Material -Packaging Material, In Process-Finished Product, Method Verification Protocol preparation & Document Section Knowledge required; Water sampling/testing, EM Observation, Culture Handling, Media Management, Having Digital exposure for LIMS/ MODA Software B.Sc/ M.Sc/ B.Pharm; Lead QC operations as Shift In-Charge. Review analytical data, Ensure compliance with LIMS, GLP, ALCOA ICH/FDA