Job Description:
Testing and Analysis: Perform routine and non-routine testing of raw materials, in-process samples, and finished products using HPLC (High-Performance Liquid Chromatography) and GC (Gas Chromatography) to ensure they meet quality specifications.
• Documentation: Maintain accurate and detailed records of all testing and analysis results. Ensure compliance with SOPs (Standard Operating Procedures) and regulatory requirements.
• Equipment Calibration: Conduct regular calibration and maintenance of HPLC and GC equipment. Troubleshoot and resolve any equipment issues.
• Compliance: Ensure adherence to GMP (Good Manufacturing Practices) and other regulatory guidelines. Participate in internal and external audits as required.
• Reporting: Prepare and review QC reports, and communicate findings to relevant departments. Assist in the preparation of regulatory submissions.
• Continuous Improvement: Identify opportunities for process improvements and contribute to the development of new QC methods and procedures.
Qualifications:
• Education: Bachelor's or Master's degree with a focus on chemistry.
• Experience: 0 to 6 years of experience in a Quality Control role, preferably within the pharmaceutical or biotechnology industry
Benefits:
Lunch Provided
Health insurance
Provident Fund
Yearly bonus
Schedule: Rotational shift