O

Officer - QC

Global Calcium Pvt. Ltd. 4.9

3–5 Years | Salary Not Disclosed | Hosur
Full Time
Posted: 14 Aug 2026 Applicants: 0

General

Work from Office

1

Any

Not Required

No

Job Description

Perform routine chemical and physical analysis of raw materials, in-process samples, and finished products.

Operate and maintain sophisticated analytical instruments such as HPLC, GC, UV-Vis, IR, etc.

Ensure accurate laboratory documentation, complete data integrity, and error-free analytical logs.

Follow current Good Manufacturing Practices (cGMP) and Good Laboratory Practices (GLP) guidelines strictly.

Support senior analysts in analytical method validation routines and sample stability studies.

Maintain complete QC test registers, calibration logs, and raw data worksheets.

Contact Details for Application:

Email: mounika.d@globalcalciumpharma.com

Qualifications

M.Sc Chemistry.

2 – 5 Years of experience in pharmaceutical or chemical Quality Control (QC) operations.

Practical hands-on expertise with HPLC, GC, UV, IR instruments, cGMP, and GLP standards.

Key Skills

HPLC GC UV IR Raw Material Analysis In-Process Testing Finished Product Testing cGMP GLP Data Integrity Method Validation
Deadline: 30 Sep 2026

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