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Responsibilities: Lead and manage day-to-day pharmaceutical manufacturing operations in compliance with GMP requirements. Develop, maintain, and control Batch Records (BR) for all production activities in accordance with GMP and FDA standards. Coordinate qualification and validation activities with QA/QC teams and external contractors. Create, update, and train employees on production documentation and Standard Operating Procedures (SOPs). Support and participate in self-inspections and continuous compliance programs. Monitor production KPIs, productivity, efficiency, quality, and cost performance. Drive cost reduction and process improvement initiatives. Manage technology transfer and product transfer projects between HQ and local manufacturing sites. Support departmental and organizational objectives as assigned by the Director. Qualifications: Bachelor's Degree in Pharmacy. More than 10 years of pharmaceutical manufacturing experience. At least 5 years of people management experience. Strong knowledge of: GMP Quality Systems Safety Management FDA compliance requirements Excellent English communication skills, both written and verbal.