Responsibilities :
Oversee and optimize pharmaceutical manufacturing processes, ensuring compliance with industry standards and regulatory requirements.
Ensure adherence to GMP, GDP, and other pharmaceutical regulations, including ISO standards, across all manufacturing activities.
Support and execute process validation activities, including the development and implementation of IQ, OQ, and PQ protocols.
Maintain detailed and accurate documentation of manufacturing processes, validations, and quality checks.
Collaborate with teams across different manufacturing sites, ensuring consistent quality and process adherence.
Identify opportunities for process improvements and implement strategies to enhance efficiency, quality, and safety in manufacturing.
Conduct quality checks and audits to ensure products meet all necessary standards and specifications.
Work closely with cross-functional teams, including R&D, Quality Assurance, and Operations, to support project goals and timelines.
Requirements :
years of experience in pharmaceutical manufacturing or a related field.
Bachelor's degree in engineering, Pharmaceutical Sciences, or a related discipline.
Strong knowledge of GMP, GDP, process validation, and regulatory requirements in the pharmaceutical industry.
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