Qc
1 week ago
**Key Responsibilities**:
- **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 in Pharmacy (B. Pharmacy / M. Pharmacy) or Science (MSc) with a focus on chemistry or a related field.
- **Experience**: 2 to 6 years of experience in a Quality Control role, preferably within the pharmaceutical or biotechnology industry.
- **Skills**:
- Proficiency in using HPLC and GC equipment.
- Strong understanding of quality control procedures and regulations.
- Excellent attention to detail and analytical skills.
- Ability to work independently and as part of a team.
- Effective communication and documentation skills.
**Job Types**: Full-time, Permanent
**Experience**:
- total work: 2 years (required)
Work Location: In person
Application Deadline: 06/09/2024
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