Job Description
Skills:
GMP Compliance, Quality Assurance, Pharmaceutical Manufacturing, Quality Control, Documentation, Regulatory Compliance, Batch Record Review, Root Cause Analysis,
GMP Compliance, Quality Assurance, Pharmaceutical Manufacturing, Quality Control, Documentation, Regulatory Compliance, Batch Record Review, Root Cause Analysis,
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
- 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.
- 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.