Sun Pharmaceutical Industries, Inc.
Sr Executive Quality Control
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📍 Bengaluru
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Job at a Glance
- Category
- MIS Executive
- Location
- Bengaluru, Karnataka, India
- Salary
- Check with seller
- Job Type
- Full Time
- Company
- Sun Pharmaceutical Industries, Inc.
- Status
- Open & Active
Job Description
Title: Sr Executive - Quality Control
Date: Sep 7, 2026
Location: Bangalore - Plant
Company: Sun Pharmaceutical Industries Ltd
Main purpose of the Job:
Should have experience on analytical methods for Biosimilars/therapeutic proteins. Responsible for analysis, documentation of quality control activities which includes in process sample, Release samples, Stability studies sample analysis for Biological products.
Job Responsibilities:
• Experience on Biosimilars mabs QC analysis.
• Protein analysis by HPLC, ELISA, OD280 methods and electrophoresis methods.
• Operation of HPLC, UV spectrophotometer, gel doc and stability chambers.
• Raw materials maintenance, preparation of specifications, CoAs.
• Sample receiving, withdrawal, aliquoting and allotting A.R.No.of In -process, batch release and stability for analysis related to products testing.
• Preparation of standard operating procedures, specification and standard testing procedures.
• Preparation of reagents, chemicals and buffers as per the STPs
• Documentation of analytical data and preparation of STP.
• Responsible for compliance to cGMP practices and maintenance of chemical inventory.
• Environmental monitoring for clean rooms in QC and manufacturing area.
• Calibration of instruments and equipment as per the SOP.
• Preparation of QMS documents like change controls, deviations etc.
Skills/Competencies
Technical Skills/Competencies (experience with Analytical Technics on Biosimialrs etc.)
Behavioral Skills/Competencies (e.g. excellent communication skills, strong collaborator, Problem solving etc
Date: Sep 7, 2026
Location: Bangalore - Plant
Company: Sun Pharmaceutical Industries Ltd
Main purpose of the Job:
Should have experience on analytical methods for Biosimilars/therapeutic proteins. Responsible for analysis, documentation of quality control activities which includes in process sample, Release samples, Stability studies sample analysis for Biological products.
Job Responsibilities:
• Experience on Biosimilars mabs QC analysis.
• Protein analysis by HPLC, ELISA, OD280 methods and electrophoresis methods.
• Operation of HPLC, UV spectrophotometer, gel doc and stability chambers.
• Raw materials maintenance, preparation of specifications, CoAs.
• Sample receiving, withdrawal, aliquoting and allotting A.R.No.of In -process, batch release and stability for analysis related to products testing.
• Preparation of standard operating procedures, specification and standard testing procedures.
• Preparation of reagents, chemicals and buffers as per the STPs
• Documentation of analytical data and preparation of STP.
• Responsible for compliance to cGMP practices and maintenance of chemical inventory.
• Environmental monitoring for clean rooms in QC and manufacturing area.
• Calibration of instruments and equipment as per the SOP.
• Preparation of QMS documents like change controls, deviations etc.
Skills/Competencies
Technical Skills/Competencies (experience with Analytical Technics on Biosimialrs etc.)
Behavioral Skills/Competencies (e.g. excellent communication skills, strong collaborator, Problem solving etc
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