About the Company
The firm is more than 200 years of experience in producing the quality standards helping major bio-pharmaceutical firms in delivering high quality medicines to relieve many diseases. This is an organization supplying methods at free of cost for the product development and maintaining the standards. This is distributed across the globe serving mankind.
About the Job
Experience required : 4-5 years experience with PhD or 7-9 years of experience with Masters in Pharma or chemistry
Candidate Need to have experienced in delivering the projects on time and with quality
Candidate need to have experienced with you With UV, thermal analysis, titrations, Karl Fischer.
Need to have experienced with Ellen QR coding system Need to handle the projects individually.
Required to have experience with high volume pharmaceutical manufacturing quality control laboratory or contract pharmaceutical organization experience
Role and responsibilities
Need to actively Taking up any additional responsibilities assigned by group leader from time to time.
Need to handle the calibration of the equipment as per the schedule and Able to perform the Executing the analytical tests allotted by Project or Group Leader.
Necessary to Coordination with group leader to ensure completion of the projects allotted to the team.
Always required to Ensure that the chemicals and column etc. are available for the projects and forward the purchase requisitions.
Able to provide the timely Supporting Verification, GPH, PQM, stability and other departmental teams in terms of testing and project review whenever needed.
Handling the sample tracking and chemical inventory tracking in the laboratory.
Able to Ensure all lab safety and GLP practices are maintained in the lab and participate actively in the internal and external audits and certification
Able to review of the project reports and documents and assisting the group leader when required.
Required to Complete the project as per the timelines and trouble shoot the scientific aspects of the projects on need basis.
Prepare and review of SOP’s, protocols, reports etc.
Identify and perform the Verification of test protocol and giving test kit approvals, if required.
Timely drafting, executing and completing IQ/OQ/PQ of new instruments.
Required to prepare the of project evaluation reports.