Officer

Job Description

•    Review of various quality system documents. 
•    Preparation and review of Standard Operating Procedures. 
•    Preparation and review of Annual product quality review reports. 
•    Handling of QAMS activities like change control, OOS, OOT, Deviations, Lab Incidences and CAPA etc. 
•    Preparation and review of quality risk management. 
•    Review of batch manufacturing record and batch packing records. 
•    Preparation and review of Standard Operating Procedures. 
•    Review, assessment and closure of other QAMS documents whenever required. 
•    Issuance and retrieval of SOP, various list, protocols and logbooks etc. 
•    Maintain all cGMP records. 
•    Management of control sample area. 
•    Review of validation and qualification documents. 

Work Experience

2-5 years

Education

Competencies