Job Description
Description:
To ensure compliance with cGLP regulations by analysis and calibration of all aspects of Quality Control at the manufacturing site
- To work as key core team member for LIMS activities.
- Preparation, Updation of masters in LIMS.
- To update the various modules available in LIMS (Caliber LIMS).
- Training, coordination and troubleshooting while routine LIMS activity in the laboratory during day-to-day activity.
- To maintain all the LIMS related documents adequately.
- To prepare the in-house protocol and report.
- To prepare the stability data summary reports
- Activities other than defined in the Job responsibility are to be done as per the requirement of HOD, by following HOD's instruction and guidance.
Education:
- Bachelors Degree (BA/BS/ B Com) B. Pharm - Required
- Master Degree (MS/MA) M. Sc. - Preferred
- Master Degree (MS/MA) M. Pharm - Preferred
Experience:
- 2 years or more in 2 - 4 Years
Specialized Knowledge: Licenses: