Quality Control (QC) – Sr. Executive

Perform sampling, analytical testing, and instrumental analysis of raw materials, in-process samples, finished products, and stability samples in an injectables formulation facility.

Operate and calibrate sophisticated QC analytical instruments including HPLC, GC, UV-Vis Spectrophotometers, and dissolution apparatus following standard pharmacopoeia methods (IP/BP/USP).

Maintain strict adherence to Good Laboratory Practices (GLP), Current Good Manufacturing Practices (cGMP), and sterile/injectable manufacturing compliance standards.

Conduct method validation, method transfer, and analytical equipment qualification protocols.

Review analytical test data, investigate Out of Specification (OOS) and Out of Trend (OOT) results, and initiate appropriate CAPA measures.

Prepare, update, and maintain comprehensive laboratory documentation, Standard Operating Procedures (SOPs), test logs, and raw data sheets for regulatory compliance.

Work Schedule, Compensation & Benefits:

Joining: Immediate joiners will be preferred

WhatsApp Application: 7032837394 (Send resume)

Email Application: ramakrishna.reddy@sanzyme.com

B.Pharm / B.Sc (Chemistry / Analytical Chemistry / Life Sciences).

6 to 8 Years of hands-on Quality Control experience specifically within an Injectables / Sterile Formulation manufacturing unit.

Gender: Male candidates preferred.

In-depth understanding of regulatory audit requirements, sterile injectable standards, and data integrity compliance.