Team Member - Microbiology
IndiaFull-time3–7 yrsPosted 3 weeks ago
Mid-level pharma role at Cipla. Needs 3+ years.
About the role
Initiate investigations and take necessary corrective and preventive actions Document entries, raw data and findings concomitantly in relevant test data sheets so as to facilitate the lab QA to review the reports and avoid missed entries Availability of Validation records of analysis samples becomes a challenge in cases where validation is performed on other sites.
What you'll do
- Analyse and review samples based on work allocation to meet the service level agreement
- Analyse samples as per priority and work allocation
- Review the data as per respective specification, Microbiological Methods and results obtained
- Investigate incidence & lab error on priority basis so that batch release timely and issues are not recurring
- Review reports as per cGMP & GDP for compliance to GLP
What you need
- Microbiology
- GMP
- GLP
- SOP writing
- SAP
- Communication