Greetings from Hetero

Walk-in Interview

OSD Production/Quality Control Departments for Hetero Formulation Unit-V Jadcherla

Interview Venue: Hetero Labs Limited Unit-V , TSIIC Pharma SEZ, Polepally Village Jadcherla-509202.

Location map: https://maps.app.goo.gl/tufbxJ9SD7F2vnV57

Interview Date:07th December 2024, Time: 09:30 AM to 03:00 PM

Production Job Responsibilities

Production Operation:

• Operate and maintain production equipment such as tablet presses, capsule fillers, coating machines, blenders, and granulators.
• Monitor and control the processing of raw materials, mixing, granulation, drying, compression, coating, and packaging.
• Perform in-process checks to ensure that products meet established specifications (e.g., weight, thickness, hardness, dissolution).

Compliance and Documentation:

• Follow GMP, SOPs (Standard Operating Procedures), and batch records to ensure the proper manufacturing of OSD products.
• Document all production activities accurately and timely in batch records, logs, and equipment logs.
• Ensure adherence to safety protocols and regulatory guidelines, including environmental and health regulations.

Quality Control Job Description

1. Quality Control Testing:

• Perform routine testing on raw materials, in-process samples, and finished products to ensure they meet quality standards.
• Use various analytical techniques and equipment such as HPLC (High-Performance Liquid Chromatography), UV spectrophotometry, dissolution testing, friability testing, hardness testing, and moisture content testing.
• Test physical properties of tablets and capsules (e.g., weight variation, hardness, dissolution, disintegration).
• Conduct microbiological testing on products, if applicable, to ensure compliance with sterility or microbial limits.

2. Raw Material and In-Process Control:

• Verify the identity, strength, and purity of raw materials before production begins.
• Perform in-process testing to ensure product consistency during the manufacturing process (e.g., weight variation checks, moisture content, granule uniformity).
• Participate in the review of batch records to ensure that all materials and processes are aligned with the defined quality specifications.