Talentmate
India
10th September 2026
2609-6430-498
• Follow cGMP and GLP PRACTICES. • To ensure current good laboratory compliance and ensuring all SOPs related to Quality Control laboratory are prepared and reviewed / implemented properly. • To follow safety Procedure in QC department. • To manage an accurate, reliable, efficient and timely review of finished products, in process/ validation, raw material, stability, GLP, Non-routine samples. • To ensure timely review of batch audit trail, system audit trail, message center. • To ensure review of Logbooks of instrument, equipment’s, columns, standards, impurities etc. • To review the COA of finished product in LIMS after the completion of analysis. • To ensure the status label updated for the instruments, equipment, glassware and workplace. • To conduct the training program to analyst as per the training calendar. • To ensure the training about the changes in standard operating procedures (SOP), if required. • To ensure the Sequence of HPLC/GC/IC are reviewed prior to start of the sample set. • To ensure methods are prepared accordingly STP/SOP. • To ensure proper integration and reviewed prior to E- signature of data by reviewer • To do any other Work assign by HOD.
| Role Level: | Mid-Level | Work Type: | Full-Time |
|---|---|---|---|
| Country: | India | City: | Dholka ,Madhya Pradesh |
| Company Website: | https://www.cadilapharma.com/ | Job Function: | General Management |
| Company Industry/ Sector: |
Pharmaceutical Manufacturing | ||
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