Job Opportunities at Baxter R&D Center
Quality Assurance
Ensuring Product Excellence
- Injectable IPQA: Oversee the quality of injectable pharmaceutical products during the manufacturing process.
- In-process Quality Check: Conduct inspections and tests to ensure products meet quality standards at various stages of production.
- Batch Release: Ensure batches of products meet regulatory requirements before release for distribution.
- Line Clearance: Verify that production lines are free from any contamination or residue before starting a new batch.
- Batch Record Review: Review and approve batch records to ensure accuracy and compliance with procedures.
Quality Control
Upholding Stringent Standards
- Analyst – GLP: Perform tests following Good Laboratory Practices (GLP) to maintain quality control standards.
- Stability: Conduct stability testing to assess the shelf-life and quality of pharmaceutical products.
- RM-PM FP: Test raw materials and packaging materials to ensure they meet specifications for final product manufacturing.
- Lab Instrument Knowledge: Proficiency in operating laboratory instruments such as High-Performance Liquid Chromatography (HPLC), Gas Chromatography (GC), Karl Fischer (KF) titrators, etc.
- QMS: Implement and maintain Quality Management Systems to ensure consistent quality control practices.
- QC Doc-cell: Manage and maintain documentation related to quality control activities.
Microbiology Lab
Safeguarding Against Microbial Contamination
- Analyst: Conduct microbiological tests to assess product safety and quality.
- Microbial Limit Test: Determine the microbial content of pharmaceutical products to ensure compliance with regulatory standards.
- Bioburden Endotoxin Test: Assess the level of microbial contamination and endotoxin presence in pharmaceutical products.
- Environment Monitoring: Monitor and control environmental conditions to prevent microbial contamination in the manufacturing facility.
- GLP: Adhere to Good Laboratory Practices to ensure accuracy and reliability of microbiological test results.
- Sterility Test: Verify the absence of viable microorganisms in sterile pharmaceutical products.
Job Details:
- Location: Ahmedabad, Gujarat
- Experience: 2 to 6 Years
- Education: M.Pharm / M.Sc / B.Pharm / B.Sc
Walk-in Interview Details:
- Date: 06th and 7th April 2024
- Time: 09:00 am to 03:00 pm
- Venue: Baxter R&D Center, Prestige Shanti Niketan, Crescent 2, Floor- 9. Thigalarapalya, Hoodi, Bengaluru, Karnataka 560067, India
Join us at Baxter R&D Center to contribute to the assurance of pharmaceutical quality and patient safety through meticulous quality assurance, quality control, and microbiological testing practices.
