Monitor the production activities in a shift by maintaining cGMP and safety norms to achieve production targets
Accountabilities
I. Monitor production activities in a shift by managing available resources to achieve production target
II. Maintain and monitor standard process parameters as per BMRs and other supporting documents for achieving production target and maintaining quality
III. Prepare manufacturing records and update online documentation to meet production and cGMP requirements
IV. Ensure that safe work processes are followed and safety appliances are utilised during production activities in shifts to create a safe working environment
V. Identify the deficiencies/errors and propose new ideas and suggest improvements to reduce the complexity in processes
Education Qualification
Bachelor in Pharmacy
Relevant Work Experience
5-6 years of experience with 2-3 years of experience in pharmaceutical manufacturing
Competencies/Skills
Rangpo
Shift Hours
Cipla Limited is an Indian-based pharmaceutical company. The Company is focused on developing new formulations for existing and new drug substances. During the fiscal year ended March 31, 2008 (fiscal 2008), the Company launched many drugs and formul... Read More