Executive | Nuvista Pharma 

Position: Executive, Quality Control

Requirements

Education

• Master of Pharmacy (M.Pharm)
• Master of Science (MSc) in Chemistry
• Master of Science (MSc) in Biochemistry
• M.Pharm or M.Sc. in Chemistry/Biochemistry from any reputed university

Experience

• At most 3 years
• Applicants should have experience in the following business area(s): Pharmaceutical/Medicine companies
• Freshers are also encouraged to apply

Additional Requirements

• At least 0 to 3 years of working experience in a well-known pharmaceutical Quality Control laboratory is preferred
• Knowledge of cGMP regulations such as USP/BP, WHO, TGA, MHRA, and US-FDA related to the manufacturing of sterile and non-sterile pharmaceutical products is an advantage

Responsibilities and Context

Job Responsibilities

• Conduct analytical work (i.e. raw material, intermediate, bulk, packing material, finished product, and stability studies) of products according to the specified method and perform routine chemical analysis of PW, WFI, and PS
• Prepare RM and finished product specifications, COAs, testing methods, SOPs, and registers
• Perform analysis of cleaning validation, process validation, and method validation of products
• Monitor calibration, qualification, and maintenance of QC equipment and ensure proper documentation
• Ensure that raw materials, components, products, or monitoring results that do not meet specifications or expectations are promptly investigated, risk assessed, and necessary CAPAs implemented

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