Company Jobs

Supervision of Micro Section Microbiological Analysis of Raw Material, Finished Product, Water Samples, Stability ad Hold Time study Samples. Review and Verification of Micro documents, Preparation of Protocols and SOP, QMS, Environment Monitoring Media Preparation, GPT Test, Microbial, Limit Test of Finished Product and Raw Material, Water Testing etc. - Calibration and Validation of Microbiological Instruments.

To Perform analytical activity of Development, Scale-up support, Method validation, Method transfer, Release, Stability, Drug product characterization, E&L study, In-Vitro study, routine analysis of inhalation dosage forms. M.Pharm, MSc

To monitor the Demo, Scale up, exhibit, and launch batches. To take scale up batch, Exhibit batches and work on Trouble shooting. To perform investigation for Deviation/ OOS/ OOT observed at plant.

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

Experience in IT, healthcare, or pharma; expert understanding of technology and methodologies as applied in the respective area. Good experience in technical planning, system integration, verification and validation, evaluating alternatives including cost, risk, supportability and analyses for systems total cost of ownership

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

Good knowledge of triple quodrupole mass spectrometer platforms and demonstrated operational independence on these platforms. Experience in bioanalysis of small molecules is must to have and knowledge about other modalities such as biomarkers, cyclic peptides is preferred.

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.

Drive science-based marketing strategies, focusing on PvP Product vs. Product, CvP Customer vs. Product, positioning, and differentiation to create unique brand identities. Graduation/Masters in Pharmacy / Biotechnology, with an MBA preferred. Take ownership of planning, implementing, and executing marketing activities in line with the brand’s calendar, brand plan, and Go-To-Market strategy.