Natco Pharma Limited - Walk-In Interviews for Quality Control / Microbiology on 20th Sep' 2025

 

Natco Pharma Limited - Walk-In Interviews for Quality Control / Microbiology on 20th Sep' 2025

Natco Pharma is an Indian pharmaceutical company based in Hyderabad, which makes finished dosage formulations and active pharmaceutical ingredients. It is the market leader in branded oncology medicines in India, and among the country's top three in producing hepatitis C drugs.

Walk-In Interview For Quality Control & Microbiology (OSD & Sterile). Exciting Career Opportunities at Natco Pharma Limited for the following requirements.

Explore career opportunities with NATCO Pharma Limited.

We are conducting a Walk-In Interview on 20th September 2025, Saturday, at Hyderabad for positions in our QC & Microbiology (OSD & Sterile) department.

Openings are available for the roles of Analyst - Quality Control (OSD & Sterile) and Trainee/Analyst - Microbiology (OSD & Sterile). Candidates with 3 to 5 years of relevant industry experience are invited to apply for the Analyst positions. Additionally, fresh graduates from the 2024 and 2025 batches who are passionate about building a career with NATCO are encouraged to attend.

Walk-In Interview Details:

Work Location: Kothur (Formulation Division)

Interview Date: Saturday, 20th September 2025

Time: 9:00 AM to 2:00 PM

Venue: Natco House, Road No.-2, Banjara Hills, Hyderabad 500034 (Opp. A.P. Productivity Council)

Open Positions:

Analyst - Quality Control (OSD & Sterile)

Experience: 3 to 5 Years

Qualification: B. Pharmacy / M. Pharmacy / M.Sc (Organic/Analytical/General)

Chemistry

Key Responsibilities:

Adherence to GLP, GDP, cGMP, and ALCOA+ standards.

Analysis of RM/IP/FP samples, Operation and troubleshooting of instruments such as HPLC, UV, KF, IR, and Dissolution Apparatus.

Demonstration of QC testing activities.

Trainee / Analyst - Microbiology (OSD & Sterile)

Qualification: M.Sc (Microbiology / Biotechnology)

Experience: 0 to 5 Years (freshers graduated in 2024 / 2025 are eligible)

Gender: Male candidates only (due to shift & oncology plant requirements)

Key Responsibilities:

Adherence to GLP, GDP, cGMP, and ALCOA+ standards.

Perform MLT, disinfectant validations, Operate VITEK-2, and culture handling.

Sterility testing and Environmental Monitoring activities.

Demonstration of Microbiology testing activities.