To organize and ensure microbiological analysis of raw materials and products (new & existing) as per Control
Direction/Pharmacopoeias/SOPs and to maintain proper documents (Trend Card, Certificate, etc.).
To follow the requirements of regulatory authorities and international guidelines while doing project management.
To assist Head of Quality Control in the administrative work of the laboratory as requested
To support GMP Audit, coordinate, prepare action plan on different audit issues and to follow up their implementation, identify gap analysis and report.
To establish and maintain Good Laboratory Practices and Good Manufacturing Practices (GLPs/GMPs) along with proper training as and when required.
To Prepare & up-grade standard operation procedure (SOP), control direction (CD), standard COFA format & standard format of trend card etc. according to current compendia or approved procedure.
A supportive environment with world-class training & international exposure to bring out the best in our people
Excellent work culture, team spirit & performance recognition schemes
Rapid career advancement and personal development for all high potential individuals