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Job Description
- Perform routine in-process checks during all stages of production, including blending, filling, packaging, and labeling.
- Ensure that production activities comply with Good Manufacturing Practices (GMP) and internal quality standards.
- Collect and analyze in-process samples and interpret results in coordination with QA and laboratory teams.
- Report any deviation or non-conformance found during in-process checks to the QA Section Head immediately.
- Maintain accurate and complete IPC documentation, logs, and reports as per regulatory and company requirements.
- Participate in investigations related to product quality issues and support root cause analysis.
- Cooperate with production staff to ensure corrective actions are implemented when needed.
- Contribute to continuous improvement initiatives related to quality control processes.
Job Requirements
- Bachelor’s degree in Pharmaceutical Sciences, Science (Chemistry, Microbiology, etc.) or a related field.
- Minimum 2 years of experience in IPC or QA roles, preferably in pharmaceutical or FMCG manufacturing environments.
- Solid understanding of GMP, ISO standards, and quality control protocols.
- Excellent attention to detail, documentation skills, and analytical thinking.
- Proficiency in MS Office and familiarity with ERP or quality systems is a plus.
- Strong communication and reporting skills.
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