Sun Pharmaceutical Industries Ltd
Designation : Manager
Function : Production
Functional Area : Quality Engineering
Job Role Summary : Equipment and Facility Validation, Preparation of VMP, coordinate execution, Preparation and review of validation documents
Job Profile :
- Build a cohesive Team to support Validation activity in A- 41 Mohali Location
- Equipment and facility Validation along with site Specific teams, which includes preparation, review and execution of protocols, and Master Validation documents.
- Preparation, Review and execute protocols & reports in facility involving utilities, engineering, manufacturing operation & cleaning which shall include but not limited to HVAC, water, compressed air, process/packing equipment w.r.t. qualification & validation
- To ensure that all qualification and validation protocols include critical steps / components which are to be checked and validated
- To prepare validation planner for all utilities and equipments
- To prepare, review & ensure compliance & written procedure w.r.t. validation function
- To ensure that all systems and equipments are validated as per the procedure/ requirements and calendar
Responsible for Quality Management System compliance i.e., Handling of Deviation, Investigation, CAPA and CCR
- To co-ordinate, review and manage the training needs and records as a department training coordinator (DTC)
- Responsible to perform the internal and external audit as per the site specific procedure. Any other responsibility that may be assigned from time to time
Job Requirements :
12 to 15 Yrs in Validation / Qualification of Pharma facilities in a regulated environment
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Work / Job Experience : 12-15 Years
Type of Experience : Regulated Pharma, Validation and Qualification activities
Academic Qualifications :
B.Pharm / M.Pharm