Packaging Team Leader / 包装主管
康泰伦特(上海)商贸有限公司
- 公司规模:50-150人
- 公司行业:制药/生物工程
职位信息
- 发布日期:2016-11-13
- 工作地点:上海-浦东新区
- 招聘人数:1人
- 工作经验:5-7年经验
- 学历要求:本科
- 语言要求:英语 熟练
- 职位类别:生产领班/组长
职位描述
职位描述:
SUMMARY OF ESSENTIAL FUNCTIONS:
The position is responsible for the daily operations associated with preproduction, label design and printing, packaging of clinical trial use products. Primary responsibility is to execute operations in accordance with production schedules, customer specifications and quality standards to minimize disruptions and maximize throughput. Position is responsible for effectively lead the packaging operators, schedule adherence, and execute operations. The position is focused on first-pass quality, record and investigates deviations and minimizing re-work.
SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:
? Train the packaging operators and ensure the packaging team is adequately staffed to meet product delivery requirements.
? Provide expectations, evaluation feedback, coaching assistance and career development support to direct reports.
? Provide guidance to direct staff with respect to setting production priorities.
? Responsible for day-to-day packaging to efficiently process pharmaceutical products in compliance with applicable quality standards and delivery requirements.
? Work with project team to make material specification and purchase the materials from the qualified venders.
? Work with project team and client to complete label design and printing as the project schedule.
? Lead the packaging team to execute the packaging job, ensure performance and on-time delivery to insure customer satisfaction.
? Responsible for ensuring all packaging areas are in a state of good repair and in inspection readiness state.
? Report any deviation related to packaging and assist operations manager to execute investigation and complete corrective action and preventive action.
? Responsible for following and ensuring the aseptic operation maintains compliance to Standard Operating Procedures (SOPs), Batch Records, quality standards, and safety practices.
? Assist operations manager to execute process improvement and SOPs creation and optimization.
? Support to execute necessary qualification and validation.
? Performance management including semi-annual and annual review for packaging operators.
? Ensure direct reports are properly cross-trained on all areas they may be required to work. Cognizant of this when managing the daily and forecasted schedule.
? Ensure safety processes through personal modeling of appropriate behaviors on daily operation and:
1. Safety awareness and training
2. Injury prevention and management
3. Safety policy accountability
? Other duties as assigned.
POSITION REQUIREMENTS:
Education: Bachelor degree or above in manufacturing/pharmaceuticals/supply chain or other relevant disciplines.
Experience:
? >5 years relevant work experiences gained in pharmaceuticals manufacturing/packaging/clinical supply/supply chain operations; knowledge in clinical supply will be definitely an advantage.
? Minimum 2 years experiences in taking a supervisory role in operations management including Pharm manufacturing/packaging/logistics/quality.
Knowledge/Skills:
? Have a good communication skills and leadership. Able to work under pressure.
? Have a good command of both oral and written English. Familiar with Windows office applications.
? Have experience and knowledge of MRP/ERP systems.
? Possess knowledge of cGMP regulations and practices a plus.
PHYSICAL/MENTAL REQUIREMENTS
? Mathematical and reasoning ability
? Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
? Ability to work effectively under extreme pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds. Be accessible to laboratory and pilot plant area(s) and office staff and to use required office equipment. Specific vision requirements include reading of written documents and use of computer monitor screen frequently.
? Overall about average intelligence, creative thinker with sound business judgement. Good negotiation and reasoning skills.
? Excellent written and verbal communications skills. Ability to easily learn and retain technical information.
? Excellent problem solving skills, including innovative and creative solutions.
? Well organized with ability to handle multiple activities simultaneously.
? Self-starter with the ability to work with people at all levels within Catalent and within customer organizations.
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SUMMARY OF ESSENTIAL FUNCTIONS:
The position is responsible for the daily operations associated with preproduction, label design and printing, packaging of clinical trial use products. Primary responsibility is to execute operations in accordance with production schedules, customer specifications and quality standards to minimize disruptions and maximize throughput. Position is responsible for effectively lead the packaging operators, schedule adherence, and execute operations. The position is focused on first-pass quality, record and investigates deviations and minimizing re-work.
SPECIFIC DUTIES, ACTIVITIES AND RESPONSIBILITIES INCLUDE BUT ARE NOT LIMITED TO:
? Train the packaging operators and ensure the packaging team is adequately staffed to meet product delivery requirements.
? Provide expectations, evaluation feedback, coaching assistance and career development support to direct reports.
? Provide guidance to direct staff with respect to setting production priorities.
? Responsible for day-to-day packaging to efficiently process pharmaceutical products in compliance with applicable quality standards and delivery requirements.
? Work with project team to make material specification and purchase the materials from the qualified venders.
? Work with project team and client to complete label design and printing as the project schedule.
? Lead the packaging team to execute the packaging job, ensure performance and on-time delivery to insure customer satisfaction.
? Responsible for ensuring all packaging areas are in a state of good repair and in inspection readiness state.
? Report any deviation related to packaging and assist operations manager to execute investigation and complete corrective action and preventive action.
? Responsible for following and ensuring the aseptic operation maintains compliance to Standard Operating Procedures (SOPs), Batch Records, quality standards, and safety practices.
? Assist operations manager to execute process improvement and SOPs creation and optimization.
? Support to execute necessary qualification and validation.
? Performance management including semi-annual and annual review for packaging operators.
? Ensure direct reports are properly cross-trained on all areas they may be required to work. Cognizant of this when managing the daily and forecasted schedule.
? Ensure safety processes through personal modeling of appropriate behaviors on daily operation and:
1. Safety awareness and training
2. Injury prevention and management
3. Safety policy accountability
? Other duties as assigned.
POSITION REQUIREMENTS:
Education: Bachelor degree or above in manufacturing/pharmaceuticals/supply chain or other relevant disciplines.
Experience:
? >5 years relevant work experiences gained in pharmaceuticals manufacturing/packaging/clinical supply/supply chain operations; knowledge in clinical supply will be definitely an advantage.
? Minimum 2 years experiences in taking a supervisory role in operations management including Pharm manufacturing/packaging/logistics/quality.
Knowledge/Skills:
? Have a good communication skills and leadership. Able to work under pressure.
? Have a good command of both oral and written English. Familiar with Windows office applications.
? Have experience and knowledge of MRP/ERP systems.
? Possess knowledge of cGMP regulations and practices a plus.
PHYSICAL/MENTAL REQUIREMENTS
? Mathematical and reasoning ability
? Ability to interpret a variety of instructions furnished in written, oral, diagram, or schedule form.
? Ability to work effectively under extreme pressure to meet deadlines. Individual may be required to sit, stand, walk regularly and occasionally lift 0-15 pounds. Be accessible to laboratory and pilot plant area(s) and office staff and to use required office equipment. Specific vision requirements include reading of written documents and use of computer monitor screen frequently.
? Overall about average intelligence, creative thinker with sound business judgement. Good negotiation and reasoning skills.
? Excellent written and verbal communications skills. Ability to easily learn and retain technical information.
? Excellent problem solving skills, including innovative and creative solutions.
? Well organized with ability to handle multiple activities simultaneously.
? Self-starter with the ability to work with people at all levels within Catalent and within customer organizations.
职能类别: 生产领班/组长
公司介绍
Catalent Overview
We are a global leader in providing integrated services, superior drug delivery technologies and manufacturing solutions to help life science innovators develop and launch successful pharmaceuticals, biologics and consumer health products. We have built an advanced range of technologies and capabilities and are dedicated to enabling a better and faster customer journey from product development to patient.
With over 85 years of experience in the industry, Catalent supports our partners in introducing 200 new products and manufacturing over 70 billion doses each year. We became a publicly traded company (NYSE: CTLT) in 2014 and have grown to become a vibrant community of more than 11,000 employees supporting over 7000 products for over 1000 customers all around the world. At Catalent, we share a common goal, to put patients first and help people around the world live better and healthier lives.
Currently, Catalent has invested in two facilities in Shanghai, China, located in Waigaoqiao FTZ and Pudong Tangzhen, is near by China’s Zhangjiang Pharma Valley area. The two clinical supply centers will work together to provide a comprehensive range of clinical supply services to clients in China, Asia Pacific and around the world.
Catalent. More products. Better treatments. Reliably supplied.™
For more information please visit our website ****************
康泰伦特概览
我们是临床研发和给药技术的全球领导者,从药物研发,商业化生产到全球服务,我们的技术和服务贯穿于产品的整个生命周期,配方前期研究到生产供应的每一个阶段,我们都能提供完善的方案服务,助力提供更好的产品疗效,让每个人的生活更健康,更精彩。
康泰伦特拥有85年的行业服务经验,每年支持我们的合作伙伴推出200+新产品,超过700亿的年产量。康泰伦特是一家朝气蓬勃的公司于2014年上市并发展成为在全球拥有11,000名雇员,为全球1000多家客户提供7000多款产品。在康泰伦特我们的核心价值观是患者***,在全世界范围内,运用专业知识和先进技术和客户合作提高和改善患者生活。
目前,康泰伦特已在中国上海投资了两家临床供应中心,分别位于外高桥保税区和毗邻张江药谷的浦东唐镇,满足客户国内外临床试验的差异化需求。两家临床供应中心将共同协作为中国、亚太以及全球客户提供全面广泛的临床供应服务。
康泰伦特。更多的产品。更好的治疗。可靠地供应。™
获取更多信息请浏览公司官网 ****************
We are a global leader in providing integrated services, superior drug delivery technologies and manufacturing solutions to help life science innovators develop and launch successful pharmaceuticals, biologics and consumer health products. We have built an advanced range of technologies and capabilities and are dedicated to enabling a better and faster customer journey from product development to patient.
With over 85 years of experience in the industry, Catalent supports our partners in introducing 200 new products and manufacturing over 70 billion doses each year. We became a publicly traded company (NYSE: CTLT) in 2014 and have grown to become a vibrant community of more than 11,000 employees supporting over 7000 products for over 1000 customers all around the world. At Catalent, we share a common goal, to put patients first and help people around the world live better and healthier lives.
Currently, Catalent has invested in two facilities in Shanghai, China, located in Waigaoqiao FTZ and Pudong Tangzhen, is near by China’s Zhangjiang Pharma Valley area. The two clinical supply centers will work together to provide a comprehensive range of clinical supply services to clients in China, Asia Pacific and around the world.
Catalent. More products. Better treatments. Reliably supplied.™
For more information please visit our website ****************
康泰伦特概览
我们是临床研发和给药技术的全球领导者,从药物研发,商业化生产到全球服务,我们的技术和服务贯穿于产品的整个生命周期,配方前期研究到生产供应的每一个阶段,我们都能提供完善的方案服务,助力提供更好的产品疗效,让每个人的生活更健康,更精彩。
康泰伦特拥有85年的行业服务经验,每年支持我们的合作伙伴推出200+新产品,超过700亿的年产量。康泰伦特是一家朝气蓬勃的公司于2014年上市并发展成为在全球拥有11,000名雇员,为全球1000多家客户提供7000多款产品。在康泰伦特我们的核心价值观是患者***,在全世界范围内,运用专业知识和先进技术和客户合作提高和改善患者生活。
目前,康泰伦特已在中国上海投资了两家临床供应中心,分别位于外高桥保税区和毗邻张江药谷的浦东唐镇,满足客户国内外临床试验的差异化需求。两家临床供应中心将共同协作为中国、亚太以及全球客户提供全面广泛的临床供应服务。
康泰伦特。更多的产品。更好的治疗。可靠地供应。™
获取更多信息请浏览公司官网 ****************
联系方式
- Email:recruiter.china@catalent.com
- 公司地址:地址:span外高桥保税区