杭州招聘

JOB SUMMARY
Supervise cGMP compounding and sterile filling operation for overall APA. Maximize efforts to lead the filling group to achieve production and quality objectives. Provide the guide line cross overall APA function.

ESSENTIAL DUTIES AND RESPONSIBILITIES
Productivity 30%
1. Supervise and continuously motivate overall 4 shifts both in compounding and filling operators to produce high quality with high efficiency and low-cost objectives.
2. Establish and maintain effective relationships with key partner, such as, packaging, Engineering, planning, and Quality. Continuously optimize and improve production work flow to achieve the organization assigned target of overall APA function.

Quality 30%
3. Continuously monitoring the aseptic process to ensure the environmental of production area consistently meet associated regulations and enterprise requirement. Ensure operator whom worked in clean area is following the required behaviors.
4. Ensure all the operation within filing, compounding and related process, is accordance with effective procedure. Identify and Establish appropriate action to solve the potential risks that might impact product quality.
5. Ensure all quality related document and record is well retained, make sure the records are right at the first time.
6. Responsible for organization appropriate resources to investigate non conformities. Establish appropriate corrective actions and preventive actions to ensure non conformities can be fixed forever.

Personnel development 20%
7. Be responsible for the continuous development of Key talent within APA team.
8. Establish and maintain appropriate personal development process in APA function, to motivate operator to maintaining in high performance level.
9. Personnel engagement: motivate both filling and compounding operators through proper goal setting and timely positive feed back based periodically performance review.

Other Responsibilities 20%
10. Ensure EHS compliance within overall APA team. And continuously to keep the operator working under a safe condition.
11. Other tasks assigned by manufacturing manager.
12. Communicate with other functional department efficiently, transparently to ensure robustness production process.

EDUCATION AND EXPERIENCE
1. College graduates or above. Pharmaceutical or medical device related background is preferred.
2. 3 years pharmaceutical or medical device production experience, 2 years management experience or equivalent. Deep understanding of clean room behavior and the processing.

ESSENTIAL SKILLS AND ABILITIES
1. Good interpersonal and communications skills
2. Good leadership
3. Good trouble-shooting or problem solving skills
4. Good computer skills, especially on MS office software
5. Good English skill on reading and writing is preferred

眼力健(杭州)制药有限公司，坐落于下沙杭州经济技术开发区于1995年开始建造，1998年投产运营。是眼力健独家投资三千多万美元建造的生产护眼系列产品的工厂。

目前工厂已经获得了ISO全球23个国家和地区的准入批准，其中包括美国的FDA和加拿大的Health Canada以及中国的GMP。公司拥有行业领先的设备，按照无菌医药产品的标准生产。目前年产量约为5500万瓶。其中齐能品牌系列产品作为总公司隐形眼镜护理液的主打产品，以其特有的品质倍受中高收入群体的青睐。公司大部分产品出口到日本、美国、欧洲及亚太其他国家和地区。

满足不同年龄层客户的需求，是眼力健全体员工的奋斗目标。

我们的产品：隐形眼镜护理液包括全能系列智护系列，双氧水产品和Purite盐溶液，以及滴眼剂。销往国家和地区：产品销往日本、加拿大、美国、中国香港、新加坡、马来西亚、印度尼西亚、韩国、澳大利亚、新西兰、中国等。