Vacancy for M.Pharm, M.Sc, B.Pharm in QC Department at Gufic Biosciences Limited

Gufic Biosciences Limited, is Research based pharmaceutical company, recognized for its innovative, high quality and 4lr fastest growing company among the top 100 companies in India. Gufic is one of the largest manufacturers of lyophilized in India with wide range of products in various therapy areas.

Post : Officer/Sr. Officer/ Executive, Department – QC (32 Posts)

Job Description
• Responsible to operate and analyze of raw materials, In Process, cleaning samples, samples for vendor qualification, Stability samples, standard and Finish product Samples and instrumental method (High performance liquid chromatograph (HPLC) / Ultra performance Liquid chromatograph (UPLC) / Gas Chromatograph (GC) and to perform analysis of process validation.
• Responsible for Daily verification of analytical balance and daily temperature monitoring. Online entry in logbooks of instrument, column, working standard, chemical inventory whenever use.
• Responsible for in process data review in night shift.
• Finished product sample receive, entry taken in register and maintain daily status.
• Responsible to follow all the Standard operating procedures, to give Instructions for housekeeping, cleaning and maintaining the laboratory area.
• Responsible to follow all the analytical procedures and generates online raw data, Chromatograms, calculation sheets and charts with reviewer signature.

• Responsible to control and maintain records like protocols, Specification, Standard test procedure, Analytical work record, Standard operation procedure, In- process analysis records, usage log books and status labels during day to day Analysis.
• Responsible to perform calibration and maintain its records.
• Responsible to Prepare and maintain record of finished product.
• Responsible to maintain record of chemicals, glass wares and other lab items of department.
• Responsible for cleaning, maintenance, and daily calibration of specified instruments.
• Responsible to maintain records and qualification of primary standards, reference standards and working standards.
• Responsible for reporting to senior if any abnormality observed during analysis and perform for the out of specification and to investigate the OOS (Out of specification) or OOT (Out of trend)if found and Responsible for maintaining QMS related documents.
• Responsible to follow various EHS (Environment Health and safety) guideline and use appropriate PPEs (Personal protective equipments).
• To assist Head of Department for the preparation of regulatory inspection.

Additional Information
Experience : 2 To 5 Years
Qualification : M.sc/B.Pharm/M.Pharm
Industry Type : Pharma/ Healthcare/ Clinical research
Functional Area : QC
End Date : 15th September, 2021