Full Time

Quality Control

Apitoria Pharma (Aurobindo)
Visakhapatnam
₹3.5 - ₹8 LPA
Posted 17/02/2026

About the Role

Roles & Responsibilities
• Perform quality testing and analysis of API materials
• Handle and operate HPLC and GC instruments for routine and stability analysis
• Conduct raw material, in-process, and finished API testing
• Ensure accurate documentation of analytical results as per GMP requirements
• Prepare and review analytical reports and release documentation
• Maintain laboratory instruments and ensure calibration compliance
• Support OOS/OOT investigations and deviation handling
• Ensure adherence to safety and regulatory guidelines

Qualification
• Bachelor of Pharmacy (B.Pharm) / M.Sc

Experience
• 2–6 years of experience in pharmaceutical Quality Control
• Strong hands-on experience with HPLC and GC instruments
• Experience in API manufacturing environment preferred

Skills
• Strong knowledge of chromatographic techniques (HPLC & GC)
• Understanding of GMP and regulatory compliance requirements
• Good analytical and troubleshooting skills
• Experience in documentation and data integrity practices
• Attention to detail and quality-focused approach
• Ability to work in a fast-paced manufacturing environment

About the Company
Apitoria Pharma Private Limited is a wholly owned subsidiary of Aurobindo Pharma Limited, focused on high-quality API manufacturing and solvent recovery operations, supporting global pharmaceutical markets with strong regulatory compliance and operational excellence.

Walk-In Details
• Date: Thursday, 19 February 2026
• Time: 09:00 AM – 12:30 PM
• Venue: Apitoria Recover Unit (Unit 6), Plot No. 17, E-Bonangi Village, JNPC, Parawada, Visakhapatnam, Andhra Pradesh – 531019
• Note: Interviews will be conducted on a first-come, first-served basis. Candidates are advised to arrive early.

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