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. The firm / organization delivers high quality trainings that help the professionals o have in depth knowledge about the subject.
About the Job
Experience : 4-6 years of experience with working the biological products
Need to have expertise in the bioanalytical areas and should or desirable to have cGMP/cGLP area exposure
Qualification :
Need to have M. Tech or M. Pharma in relevant stream
Candidates could have MSc ( Bio chemistry/ biotechnology, analytical chemistry or instrumentation)
or can have M. tech or M. Pharma and able to handle the HPLC, UPLC, spectrophotometry, electrophoresis (SDS-Page, western blot)
Need to have good communication and writing skills
Should have strong technical background on mass spec for qualitative and quantitative analysis.
Need to have strong experience with the HRMS and MS relevant sample preparation
JD
Able to follows and ensures aspects related to safety, ethics, and legal compliance
Need to Prepare project reports as per USP’s quality systems and procedures
Should be able to demonstrates strong skills and expertise in Bioanalytical methods in the areas of Mass spectrometry, Chromatography (HPLC/UPLC), Electrophoresis, Colorimetric and Enzyme assays
Candidate need to performs duties for the allocated lab/equipment’s/inventory/supporting activities and takes responsibility for the timely completion of the tasks assigned
Should be able to Complies with USP’s Quality Management System and assists group leaders in implementing process improvements
Application personal experience, academic training, and technical insights to handle and to troubleshoot and solve problems in the laboratory