Job description

Identification, logging and implementation of Global CAPA. Involvement in OOS decision making process Collect, interpret and review of the stability OOS investigation Coordinate with CFT for timely closure of stability Investigation Review & evaluation of Change request related to revision of product shelf life / storage condition / overages. Preparation of analytical allocation / monitoring tool Review / update on Quality matrix data for council meeting product approval form for new products & existing products (AVD) for timely and successful launch right at first time.

Skills Required

Key Skills

• QUALITY ASSURANCE
• ORAL SOLIDS
• ORAL LIQUIDS
• EXTERNAL AND STERILE PRODUCTS PROCESSING AND CONTROLS
• QMS
• CGMP

Other Information