Head of QC
上海任仕达人才服务有限公司
- 公司性质：合资(欧美)
- 公司行业：专业服务(咨询、人力资源、财会)
职位信息
- 发布日期：2012-08-06
- 工作地点：苏州
- 招聘人数：若干
- 工作经验：八年以上
- 学历要求：硕士
- 职位类别：质量管理/测试经理(QA/QC经理) 质量管理/测试主管(QA/QC主管)
职位描述
Role Head of QC
Location Nansha
Line Manager QA Director
Role Summary
The position is responsible for the leadership and efficient operation of the Quality Control function for the company. The candidate should establish and improve quality control systems and practices and ensure that the quality control function is in compliance with all related GMP and non-GMP quality requirements. The role is to provide Analytics support to all business units at Guangzhou-Nansha site.
Primary Role Responsibilities
1. Provide high level of leadership to the China QC group to ensure it is managed effectively and efficiently.
2. Support Operations and R&D to ensure that the developed, manufactured and delivered products are tested and released according to established procedures, and that they meet all quality requirements, where major focus lies on cGMP.
3. Establish goals, objectives and priorities. Develop and execute action plans to achieve an excellent Quality Control service platform, which is able to support Operations ranging from routine mono-production to fast changing development and production campaigns.
4. Develop, implement, maintain and continuously improve systems to ensure customer satisfaction with our products and services. To ensure compliance with government and international regulations applicable to our products and services.
5. Responsible for budget, administration, planning and related activities of QC function. Drive and implement strategies for highly cost effective business performance.
6. Establish a system to ensure that all related laboratory environments, facilities and equipments are sutainably maintained on required quality level. This includes chemical and microbiological testing equipment, facilities for stability studies and other equipments related to testing and release of pharmaceutical and chemical products.
7. Provide support for the development and validation of adequate analytical methods to fullfill the needs from R&D to full cGMP large scale production.
8. Provide a platform which can ensure effective analytical tech transfer and validation at the required quality level and providing high customer satisfaction. Main focus on pharmaceutical products (cGMP).
9. Recruit, enable, develop and retain staff, which can continuously and effectively provide quality control services.
10. Establish and keep up high safety standards in all related laboratory units.
11. Drive and support companywide global harmonization efforts regarding systems and processes.
12. Evaluate trends in analytical techniques and industry practices. Drive implementation if business and quality advantages are obvious.
13. Review technical problems and procedures of operations and recommend solutions to problems or changes in operation procedures.
14. Perform other projects or initiaties required by the company.
Quality Responsibility
Based on all related Quality requirements (cGMP, ISO etc.) of all target markets.
Safety Responsibility
Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
Requirements
1. Master degree or above
2. 8+ years of experience in chemical or pharmaceutical industry, focus on quality control environment
3. Proven strong leadership skills
4. Experience in quality control systems required for a GMP/ISO operation. Must be familiar with relevant domestic and international GMP requirements and practices.
5. High-level of integrity and code of business conduct.
6. Strong business acumen, with strategic thinking and good decision quality
7. Ability to develop clear, actionable steps in support of business objectives.
8. Strong communication and interpersonal skills, a mature relationship builder.
9. Proactive, high level of commitment and accountability.
10. An effective team player.
11. Setting clear objectives, manage team performance, motivate and develop team, demonstrate behaviour as a matured team leader.
12. Fluency in Mandarin and English (written, oral)
Working Conditions
Office environment; domestic and international travel on occasion basis; manufacturing or lab environment on occasion basis.
[Please send your resume to my mail , thank youvery much!]
gordon.ye@randstad.cn
Location Nansha
Line Manager QA Director
Role Summary
The position is responsible for the leadership and efficient operation of the Quality Control function for the company. The candidate should establish and improve quality control systems and practices and ensure that the quality control function is in compliance with all related GMP and non-GMP quality requirements. The role is to provide Analytics support to all business units at Guangzhou-Nansha site.
Primary Role Responsibilities
1. Provide high level of leadership to the China QC group to ensure it is managed effectively and efficiently.
2. Support Operations and R&D to ensure that the developed, manufactured and delivered products are tested and released according to established procedures, and that they meet all quality requirements, where major focus lies on cGMP.
3. Establish goals, objectives and priorities. Develop and execute action plans to achieve an excellent Quality Control service platform, which is able to support Operations ranging from routine mono-production to fast changing development and production campaigns.
4. Develop, implement, maintain and continuously improve systems to ensure customer satisfaction with our products and services. To ensure compliance with government and international regulations applicable to our products and services.
5. Responsible for budget, administration, planning and related activities of QC function. Drive and implement strategies for highly cost effective business performance.
6. Establish a system to ensure that all related laboratory environments, facilities and equipments are sutainably maintained on required quality level. This includes chemical and microbiological testing equipment, facilities for stability studies and other equipments related to testing and release of pharmaceutical and chemical products.
7. Provide support for the development and validation of adequate analytical methods to fullfill the needs from R&D to full cGMP large scale production.
8. Provide a platform which can ensure effective analytical tech transfer and validation at the required quality level and providing high customer satisfaction. Main focus on pharmaceutical products (cGMP).
9. Recruit, enable, develop and retain staff, which can continuously and effectively provide quality control services.
10. Establish and keep up high safety standards in all related laboratory units.
11. Drive and support companywide global harmonization efforts regarding systems and processes.
12. Evaluate trends in analytical techniques and industry practices. Drive implementation if business and quality advantages are obvious.
13. Review technical problems and procedures of operations and recommend solutions to problems or changes in operation procedures.
14. Perform other projects or initiaties required by the company.
Quality Responsibility
Based on all related Quality requirements (cGMP, ISO etc.) of all target markets.
Safety Responsibility
Is knowledgeable and complies with all pertinent safety policies, rules and regulations.
Requirements
1. Master degree or above
2. 8+ years of experience in chemical or pharmaceutical industry, focus on quality control environment
3. Proven strong leadership skills
4. Experience in quality control systems required for a GMP/ISO operation. Must be familiar with relevant domestic and international GMP requirements and practices.
5. High-level of integrity and code of business conduct.
6. Strong business acumen, with strategic thinking and good decision quality
7. Ability to develop clear, actionable steps in support of business objectives.
8. Strong communication and interpersonal skills, a mature relationship builder.
9. Proactive, high level of commitment and accountability.
10. An effective team player.
11. Setting clear objectives, manage team performance, motivate and develop team, demonstrate behaviour as a matured team leader.
12. Fluency in Mandarin and English (written, oral)
Working Conditions
Office environment; domestic and international travel on occasion basis; manufacturing or lab environment on occasion basis.
[Please send your resume to my mail , thank youvery much!]
gordon.ye@randstad.cn
公司介绍
上海任仕达人才服务有限公司诚聘
联系方式
- Email：recruitmentsh@cn.randstad.com