Associate Production Manager-J2149406221
深圳市安仕达信息咨询有限公司
- 公司规模:50-150人
- 公司性质:外资(非欧美)
- 公司行业:专业服务(咨询、人力资源、财会)
职位信息
- 发布日期:2013-02-22
- 工作地点:武汉
- 招聘人数:1
- 工作经验:十年以上
- 学历要求:本科
- 语言要求:英语熟练
- 职位类别:生产经理/车间主任 生物工程/生物制药
职位描述
Job Description
-Under the direction of Sr. Manager mfg, the Associate Production Manager is responsible for all activities related to the mfg of the product as per formula instructions. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced.
-Communicate with others and assimilate and understand information, in a manner consistent with the essential job functions. Work independently and as part of a team. Identify, analyze, and solve problems. Follow directions and follow through with assigned tasks. Maintain a clean and safe work area. Mechanical skills. Provide on-the-job training of new employees.
-Required to competently & independently supervise within a team environment
-Plan, supervise and direct and manufacturing personnel to achieve short and long term departmental objectives, Problem solves / troubleshoots production issues and recommends / implements changes to maximize production yields and efficiencies, Ensure staff is properly trained and competent in all technical aspects of their positions.
-Complies with company policies and procedures and maintains regular work attendance.
-Actively promote and maintain a safe work environment, Establish staffing guidelines and distribute workload so as to deliver maximum results, Maintain two way dialog with direct reports on work and results, Communicate company and departmental goals and objectives assuring that these are clearly understood by the shift, Complete and maintain all necessary documentation including applicable current Good Manufacturing Practices (cGMP) documents.
-Work with Engineering Maintenance, Quality Control and other departments as needed in order to ensure adherence to Standard Operating Procedures, Quality and cGMP Standards, Administer company policies regarding attendance, conduct, performance, quality, safety and teamwork, Interacts with Quality, Planning and Engineering daily to assure production schedules are met or exceeded, Responsible for personnel development. Instruct, train, motivate and assist employees so that company and departmental objectives are achieved, other duties as assigned.
Job Requirement:
-Excellent interpersonal and communication skills - verbal and written( English and Chinese ).
-Minimum 10 years working experience in related field in a global corporation.
-Previous experience in a cGMP/FDA environment.
-Ability to set priorities and multi-task to achieve desired results.
-Excellent organization and analytical skills, Coaching and mentoring skills - development of team.
-Ability to define problems, collect data, establish facts and draw conclusions in a systematic fashion.
-Ability to interpret complex technical instructions from manuals and instruction sheets.
-Under the direction of Sr. Manager mfg, the Associate Production Manager is responsible for all activities related to the mfg of the product as per formula instructions. Also, responsible for adhering to the Standard Operating Procedures (SOPs) and Good Manufacturing Practices (cGMPs) that are in effect assuring the quality and quantity of product produced.
-Communicate with others and assimilate and understand information, in a manner consistent with the essential job functions. Work independently and as part of a team. Identify, analyze, and solve problems. Follow directions and follow through with assigned tasks. Maintain a clean and safe work area. Mechanical skills. Provide on-the-job training of new employees.
-Required to competently & independently supervise within a team environment
-Plan, supervise and direct and manufacturing personnel to achieve short and long term departmental objectives, Problem solves / troubleshoots production issues and recommends / implements changes to maximize production yields and efficiencies, Ensure staff is properly trained and competent in all technical aspects of their positions.
-Complies with company policies and procedures and maintains regular work attendance.
-Actively promote and maintain a safe work environment, Establish staffing guidelines and distribute workload so as to deliver maximum results, Maintain two way dialog with direct reports on work and results, Communicate company and departmental goals and objectives assuring that these are clearly understood by the shift, Complete and maintain all necessary documentation including applicable current Good Manufacturing Practices (cGMP) documents.
-Work with Engineering Maintenance, Quality Control and other departments as needed in order to ensure adherence to Standard Operating Procedures, Quality and cGMP Standards, Administer company policies regarding attendance, conduct, performance, quality, safety and teamwork, Interacts with Quality, Planning and Engineering daily to assure production schedules are met or exceeded, Responsible for personnel development. Instruct, train, motivate and assist employees so that company and departmental objectives are achieved, other duties as assigned.
Job Requirement:
-Excellent interpersonal and communication skills - verbal and written( English and Chinese ).
-Minimum 10 years working experience in related field in a global corporation.
-Previous experience in a cGMP/FDA environment.
-Ability to set priorities and multi-task to achieve desired results.
-Excellent organization and analytical skills, Coaching and mentoring skills - development of team.
-Ability to define problems, collect data, establish facts and draw conclusions in a systematic fashion.
-Ability to interpret complex technical instructions from manuals and instruction sheets.
公司介绍
安仕达咨询(Nstarts Consultants)是一家专注于人力资源配置与发展的咨询公司,我们为客户提供专业、精准的猎头服务与RPO服务。
我们在2004年成立于香港,2005年开始拓展大陆市场,至今已先后在深圳、广州、上海、北京、杭州、长沙、江门成立分公司。运营至今,我们拥有超过10年的人力市场运营经验,为数百家优秀企业提供过人力资源服务。目前,合作3年以上并且愿意与我们建立长期合作伙伴关系的优秀企业已超过200家。
我们拥有超过100位的专业顾问,他们专注行业发展,为客户提供专业、优质的人力资源服务。我们深入了解客户的需求与文化,了解候选人的能力与动机,为客户与人才提供***匹配方案。
如需了解更多信息,请浏览公司主页:www.nstarts.com。
请加入我们:
-安仕达的快速而稳健的发展,可为你带来更多的学习机会和上升空间。
-多名专业资深猎头顾问做导师,可让你迅速成长为专业的猎头顾问。
-与中高端人才的交流沟通,让你能够拓宽视野,提升自我。
-完善的晋升体系,给你带来公平的发展平台。
-健全的薪酬体系,可让你挑战高薪。
安仕达只接受持续学习,积极进取,不断挑战自己的成员!
我们期待不甘平庸的你加入!
我们在2004年成立于香港,2005年开始拓展大陆市场,至今已先后在深圳、广州、上海、北京、杭州、长沙、江门成立分公司。运营至今,我们拥有超过10年的人力市场运营经验,为数百家优秀企业提供过人力资源服务。目前,合作3年以上并且愿意与我们建立长期合作伙伴关系的优秀企业已超过200家。
我们拥有超过100位的专业顾问,他们专注行业发展,为客户提供专业、优质的人力资源服务。我们深入了解客户的需求与文化,了解候选人的能力与动机,为客户与人才提供***匹配方案。
如需了解更多信息,请浏览公司主页:www.nstarts.com。
请加入我们:
-安仕达的快速而稳健的发展,可为你带来更多的学习机会和上升空间。
-多名专业资深猎头顾问做导师,可让你迅速成长为专业的猎头顾问。
-与中高端人才的交流沟通,让你能够拓宽视野,提升自我。
-完善的晋升体系,给你带来公平的发展平台。
-健全的薪酬体系,可让你挑战高薪。
安仕达只接受持续学习,积极进取,不断挑战自己的成员!
我们期待不甘平庸的你加入!
联系方式
- Email:nstartshr@nstarts.com
- 公司地址:上班地址:江门