Job Responsibilities:
1. Objective & Plan Management: Formulate production targets, technical task objectives and detailed implementation plans in accordance with the company’s annual business management goals, and drive the execution and fulfillment of set targets.
2. Production Process Control: Organize and execute production schedules, coordinate and resolve on-site issues arising from production activities in real time.
3. On-time Delivery Assurance: Overall coordinate and supervise adjustments and revisions of production operation plans, establish flexible response mechanisms to ensure on-time order delivery and meet customer requirements.
4. Quality & Safety Supervision: Conduct full-process quality control on purchased semi-finished goods and finished products in strict compliance with production specifications and quality requirements to prevent non-conforming products from flowing into subsequent processes; implement work safety accountability to avoid safety incidents.
5. Process Specification Establishment: Draft and continuously optimize workshop Standard Operating Procedures (SOP) and safety regulations, organize staff training and supervise implementation to consolidate the foundation of production safety.
6. Team Management & Training: Arrange daily workload for workshop production personnel, conduct vocational skill improvement and production safety training, and build an efficient, compliant and safe production team.
Job Requirements:
1. Bachelor’s degree or above, majoring in Materials Science, Chemical Engineering and Technology or related disciplines.
2. Familiar with production process principles, quality standards and safety specifications of pharmaceutical intermediates, APIs or pharmaceutical manufacturing; equipped with systematic expertise in production management, quality management and safety management, and knowledgeable about core industry codes including GMP and work safety standardization regulations.
3. Over 5 years of working experience as production supervisor/manager, among which no less than 3 years in production operation management for pharmaceutical intermediates, APIs or pharmaceutical manufacturers, capable of independently overseeing the entire production workflow.
