Tasks, duties, and responsibilities as listed in this job description are not exhaustive. The Company, at its sole discretion and with no prior notice, may assign other tasks, duties, and job responsibilities.
B.Pharma / M.Sc. pharmaceutical manufacturing, specifically in Quality Assurance or Production. AMPS Agile Manufacturing Production System exceptions with supervisor support. pfizer
The role works under general supervision, exercises independent judgment within established processes and fosters productive internal and external relationships to resolve mutual problems and contribute to streamlined operations.
Supervise administrative and contractual staff and ensure efficiency and maintaining housekeeping checks. Handling day-to-day grievances of employees related to canteen & Transportation.
Review of R&D documents such as stability data, Analytical reports, Method verification reports, Method validation protocols & reports, analytical data of pilot bio batches / DQ batches and Product development data for its adequacy.
Maintain self-hygiene and ensure compliance with cGMP, GDP and departmental discipline. Prepare and review the master documents, protocols and reports of production as per requirements.