Dear Applicant,

We have opening for Formulation Quality Control Department.

Qualification: B. Pharm or M. Pharm or M.Sc Analytical.

Experience : 2-6 Yrs.

:

1. Responsible to perform chemical & instrumental analysis of Raw material, finished product, Stability, In-process, Process validation samples, Swab/Rinse Samples Dissolution profiles and RLD samples.
2. Responsible to perform analytical method verifications, method validations, and corresponding documentation.
3. Maintain and update analytical records with complete data derived from analysis.
4. Preparation of STPs, SOPs, Protocols, Reports & Specifications.
5. Responsible for Initiation of LIR, PNC, OOT, OOS and change controls.
6. Responsible for the maintenance of chemicals, glassware, reagents, standards (Reference, Working and Impurity standards) & Columns.
7.



Responsible for sample management i.e., Storage and destruction of samples after approval.
8. Responsible for updating and monitoring of temperature and area cleaning in QC lab.
9. Responsible for the maintenance of instrument or equipment cleanliness.
10. Responsible to follow Positive Laboratory Practices in the lab.
11. Responsible for immediate intimation to supervisor in case of any malfunctioning of the equipment or instrument, Out of trend results or Out of specification results and involving in the respective investigations.

12 Ensure compliance with GMP and ALCOA+ data-integrity principles. Note: Preferable Male candidates for shift rotation basis

📌 Walk-in || Executive or Sr Executive For Formulation QC (Hyderabad)
🏢 Zenara Pharma
📍 Hyderabad