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Title:  20220217 Production Supervisor x1

Requisition ID:  48322
Date:  Jul 3, 2022
Location: 

Shanghai, Shanghai, CN

Department:  Operations
Description: 

 

 

Working at West means having an opportunity to work by the side of our patients and customers, our global team members and the communities in which we operate – which all help contribute to a Healthier World.

 

At West, we are by the side of patients. The work we do impacts patients’ lives each and every day – our products are a critical part of healthcare delivery and we are proud of the role we play to improve patient health. We work by the side of our team members. We come together as one global team to deliver for our customers and help them address their challenges. We are a diverse, close-knit community of professionals, where everyone has a voice and opportunity to learn and grow through mutual trust and respect. With a 95 year plus history, we have a track record for success, which includes reported sales of $2.14B in 2020. We serve by the side of our community. Giving back is in our DNA—our team members across more than 50 sites globally are involved with hundreds of charities that have special meaning to them through our West Without Borders team member-led giving program.

 

Job Summary:

  • 负责监督日常运行,确保并持久地达到期望的安全生产,产品质量,生产效率及一线人员管理。

Oversee daily operation to ensure the safety, quality, productivity, and front-line people management expectation are consistently achieved.

 

  • 负责生产过程持续改进,并建立相应流程。

In charge of production process continuous improvement and establish relative procedure.

 

  • 负责生产部新员工的招聘与培训。

Responsible for new production employee hiring and training.

     

Essential Duties and Responsibilities:    

  • 保证安全生产和保持生产区域干净。

Ensure safe working environment and good housekeeping.

     

  • 制定车间作业计划,确保合理产能安排。

Develop workshop operation plan, ensure daily production in an optimal capacity mode.

     

  • 监控每日生产产量,如生产期间有异常须进行事故根因调查。

Monitor the performance of daily production output and do root case investigation in case of abnormal production.

           

  • 在生产过程中监督和转移物料到其他部门,并做好生产日常消耗品的管理工作。

Monitor and transfer work in process material to other department and take care of daily consumption management for production department..

  

  • 监督和管理每天生产活动,准备和递交每月生产报表。

Supervise the daily production activities, prepare and submit production report monthly,.

     

  • 制定和维护生产相关文件。

Develop and maintain production Standard Operating Procedures.

     

  • 培训和指导新员工使其能胜任他们的工作。

Train and develop new production operators to be effective in their jobs.

     

  • 为验证与工程建设提供支持。

Provides support to projects and validations.

             

  • 执行上司所安排的工作。

Carry out other duties as directed by superior.

 

  • 质量

Quality:  

  • 理解公司的质量政策,明白工作中与质量有关的行为准则。

The job holder is aware of her special responsibility for quality and conducts his/her activities in accordance with the Company quality policy at all times.

 

  • 保证所有相关的文件记录符合GMP要求。

Ensure results are documented in accordance to cGMP and procedure.

 

  • SOP:    

知道公司所有关于此工作职责相关的文件

Be  aware of all relevant SOPs as per Company policy as they are related  to the position covered by this Job Description

 

  • 安全

Safety:  

  • 始终遵从公司的安全健康政策

Be aware of his/her special responsibility towards health and safety in accordance with the company’s safety policy at all times;

 

  • 安全工作,不作危险性危及危害安全的工作。

Work safely by not causing unsafe conditions or doing unsafe acts

 

  •  Lean: 遵从公司精益指示

Support and contribute actively in Lean Sigma programs and activities towards delivery of the set target.

 

 

Education and Experience:

  • 具有工程或制药相等程度的大学学历文凭。

Bachelor’s Degree in engineering or pharmaceutics discipline or equivalent.

    

  • 至少5年相关工作经验,具有医疗行业工作经验尤佳。

Minimum 5 years working experience with the related industry, an advantage for working in pharmaceutical industry before.

 

  • 具有领导能力和领导技能。

Leadership skills and ability to lead.

  

  • 良好的英文沟通能力。

Good English communication skill.

 

  • 富有责任感和使命感。

Sense of responsibility and urgency.

 

Knowledge, Skills and Abilities:

  • 具有GMP工作经验

Knowledge of GMP manufacturing process.

    

  • 具有生产管理工作经验。

Experience of production supervision.

 

  • 具有医疗行业工作经验尤佳。

Knowledge of rubber technology or pharmaceutical/medical device manufacturing environment and experience in SAP PP/MM will be added advantage..

 

 

 

 

 

 

West is an equal opportunity employer and we value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sex, gender identity, sexual orientation, age, marital status, veteran status, or disability status.  If you have a special need that requires accommodation in order to apply to West, please send an email to Apply.Accommodation@westpharma.com.  Where permitted by law, an offer of employment with West Pharmaceutical Services, or any of its subsidiary or affiliate companies, is contingent upon the satisfactory completion of background screening and/or a pre-employment drug screening.

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