Website Kanghong Pharmaceutical
Deputy general manager of production
Facility Construction Period:
1、Participate in the overall design of the facility, provide independent and professional opinions and guidance for the construction of production and warehouses areas to ensure the compliance with laws and regulations.
2、Lead the systemic design of logistics system, including warehousing operation and automated information system to meet the efficiency, cost and safety goals.
3、Participate in URS development and review, and provide technical evaluation of process equipment in the early stage to ensure seamless production upon construction completion.
4、Assist the general manager in providing independent guidance for production related drawings and URS development, system installation and acceptance testing, and etc.) to ensure the efficient operation of the entire production system during operation period and minimize the quality risk.
Normal Production and Operation Period:
1、Manage production related activities including on-time product supply to the markets, supply chain and warehouse management, and etc., and achieve high level of efficiency in operations and resource utilization.
2、Establish and improve production management system and procedures. Supervise the production system to ensure its conformance to the overall quality management system.
3、Set up and implement plans for technical improvement and process optimization initiatives within the production system. Constantly strive to improve efficiency and control production costs and quality risks.
4、Set up and implement annual objectives for the production teams based on the overall corporate goals. Assign activities to individual responsible person to ensure the achievement of annual objectives.
5、Set up and implement recruitment and team building plans for the production teams, to ensure the stability and continual team development.
6、Provide leadership in the investigation of major deviations and in the implementation of CAPA measures in production related areas.
7、Be responsible for the modification and expansion projects of the production areas and ensure that the projects’ schedule and quality meet requirements.
8、Review internal and external documents and data from the production system to ensure authenticity, accuracy, completeness, and conformity to corporate requirements.
9、Manage departmental personnel within the production system to complete all required tasks to meet the needs of manufacturing and quality management, including maintenance, calibration, validation, shop floor management, and etc.
1、Bachelor degree or above in biotechnology, biochemical engineering or related fields.
More than ten years working experience in biopharmaceutical production, technology, quality or other areas.More than five years management experience in biopharmaceutical commercial manufacturing.
2、Experienced in the production management of biological drugs,Can independently lead teams to improve the efficiency and stability of processes and operations through technological innovations,Experience in sterile products is preferred.
3、Familiar with the cost control measures in each production step and area,
Proficient in GMP management, familiar with US and EU cGMP regulations, working knowledge in biopharmaceutical processes and specifications.
4、Strong execution and craftsmanship skills, able to organize and implement technological innovation projects at the corporate level.