Job Details
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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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