About the Job :
This is an independent organization, which have more than 200 years of experience. The organization delivers high quality reference standards to the globe. it supplies the monographs as a reference for the evaluation of drugs. It also have food standards wing. There are multiple labs located across the globe and is an independent body from FDA or EU. The organization have more than 5000 colleagues globally serving to deliver the high quality medicines from the pharmaceutical companies.
Job Requirements :
Qualification :
candidate need to have masters with 5-7 years or PhD with 1-2 years in pharma
Role :
Candidate need to prepare the SOP and reports, protocols and their review
Need to execute and review the IQ/OQ and PQ documents for the respective instruments
Need to complete the projects assigned within the timelines
Preparation of project evaluation reports
Performing the calibration daily for the instruments
Should track the chemical inventory and need to indent them on regular basis incase of depletion
Should adhere to the GLP and need to see all the colleagues are aligned to them
Should perform stability testing if required