Perform analysis of Raw materials, Packaging materials, Bulk and Finished pharmaceutical products.
Perform analysis of Ongoing stability study of Finished products.
Able to operate QC analytical equipment’s like IR spectroscopy, UV-Vis spectroscopy, chromatographic techniques (HPLC/GC) etc.
Create and maintain laboratory documentation as per cGMP requirement.
Comply with lab SOPs, GLP, GMP, and company safety requirements.
Perform other related duties as assigned to meet departmental and company objectives.
Age At most 32 years Minimum 2 to 3 years working experience in the required department in a GMP compliant pharmaceuticals.Good interpersonal & communication skills and ability to work under pressure.Longing for rapid career growth
https://bdjobs.com/h/details/1524780
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