Personal Health-Assembly Process Engineer
飞利浦(中国)投资有限公司 Philips (China) Investment Co.,Ltd.
- 公司规模:10000人以上
- 公司性质:外资(欧美)
- 公司行业:多元化业务集团公司
职位信息
- 发布日期:2017-07-30
- 工作地点:珠海
- 招聘人数:若干人
- 工作经验:5-7年经验
- 职位类别:产品工艺/制程工程师
职位描述
职位描述:
Your Team
This role belongs to Personal Care Production department, as 1 of the 4 Process Engineers, reports to Proudction Manager directly.
Your challenge
Trouble shooting for production related issue.
We offer
Competitive compensation, stable career development, world-class manufacturing experience and learning opportunities.
Purpose:
1. To maintain and improve the process of mass production to meet quality, efficiency, safety, cost and delivery target
2. To train & guide operator, line leader, to ensure high quality/efficiency etc.
3. To involve in project team for new project smooth launch support, achieve PIP target
4. To coordinate and or cooperate with other members related to push continuous improvement
5. To perform the equipment/process qualification and components release to ensure equipment / process/components comply with specification /requirement
Your Responsibilities:
1. To handle trouble-shooting of daily production process problem, optimize and improve production process to improve FOR/CQ &efficiency
2. To coordinate and/or cooperate with other members related to push continuous improvement,
3. Feedback and support suppliers/PPD to improve incoming material quality with SQE/PPD engineer via providing analysis result
4. To request change by issuing related document: ECN/TAN/WI
5. To train & guide operators/ new operator/ line leaders to ensure they are adequately trained to perform their assigned responsibilities according to WI or procedure.
6. To conduct or coordinate assembly test and evaluation for parts release/equipment release/ equipment revalidation.
7. To be involved in market complaint confirmation & related corrective actions
8. To be involved in Lean production improvement.
9. Involvement in IPD:
a) Early involved NPI phase: Production input in product design, process design by participate product/process FMEA/control plan /incoming material package method
b) To support sample release, engineering trial run
c) Responsible for coordinate of process trial run
d) Verify process/equipment condition for Release for Production, prepare qualification protocol and qualification report.
10. Following company relevant regulations, FDA regulation, internal standards and corporate policies, EHS policy, procedures; immediately reporting work-related injuries and illnesses; reporting unsafe conditions; etc.
We are looking for
1. Education: Bachelor degree or above, major in Mechanical engineering is preferred
2. Experience: At least 5 years work experience in manufacturing process engineering field,
3. Competency and Skills
a) Strong Process Engineering Capability, good understanding of plastic material, mould structure. Good trouble shooting skills in assembly processes.
b) Functional knowledge of statistics and related analytical tools like DOE and SPC.
c) ISO, MRP/SAP awareness and familiar with BOM.
d) Solid experience on APQP, FMEA, MSA, NPI/IPD procedure, process Validations, documentation and problem solving;
e) Profound understanding of ISO9000, ISO14001, OHASH18000, ISO13485/FDA(OHC required) and quality tools.
f) Good Communication skills, self- discipline, problem solving oriented.
g) Good command of English both writing and spoken.
h) Good computer skill at MS-office., CAD, UG.
i) Good teamwork player.
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Your Team
This role belongs to Personal Care Production department, as 1 of the 4 Process Engineers, reports to Proudction Manager directly.
Your challenge
Trouble shooting for production related issue.
We offer
Competitive compensation, stable career development, world-class manufacturing experience and learning opportunities.
Purpose:
1. To maintain and improve the process of mass production to meet quality, efficiency, safety, cost and delivery target
2. To train & guide operator, line leader, to ensure high quality/efficiency etc.
3. To involve in project team for new project smooth launch support, achieve PIP target
4. To coordinate and or cooperate with other members related to push continuous improvement
5. To perform the equipment/process qualification and components release to ensure equipment / process/components comply with specification /requirement
Your Responsibilities:
1. To handle trouble-shooting of daily production process problem, optimize and improve production process to improve FOR/CQ &efficiency
2. To coordinate and/or cooperate with other members related to push continuous improvement,
3. Feedback and support suppliers/PPD to improve incoming material quality with SQE/PPD engineer via providing analysis result
4. To request change by issuing related document: ECN/TAN/WI
5. To train & guide operators/ new operator/ line leaders to ensure they are adequately trained to perform their assigned responsibilities according to WI or procedure.
6. To conduct or coordinate assembly test and evaluation for parts release/equipment release/ equipment revalidation.
7. To be involved in market complaint confirmation & related corrective actions
8. To be involved in Lean production improvement.
9. Involvement in IPD:
a) Early involved NPI phase: Production input in product design, process design by participate product/process FMEA/control plan /incoming material package method
b) To support sample release, engineering trial run
c) Responsible for coordinate of process trial run
d) Verify process/equipment condition for Release for Production, prepare qualification protocol and qualification report.
10. Following company relevant regulations, FDA regulation, internal standards and corporate policies, EHS policy, procedures; immediately reporting work-related injuries and illnesses; reporting unsafe conditions; etc.
We are looking for
1. Education: Bachelor degree or above, major in Mechanical engineering is preferred
2. Experience: At least 5 years work experience in manufacturing process engineering field,
3. Competency and Skills
a) Strong Process Engineering Capability, good understanding of plastic material, mould structure. Good trouble shooting skills in assembly processes.
b) Functional knowledge of statistics and related analytical tools like DOE and SPC.
c) ISO, MRP/SAP awareness and familiar with BOM.
d) Solid experience on APQP, FMEA, MSA, NPI/IPD procedure, process Validations, documentation and problem solving;
e) Profound understanding of ISO9000, ISO14001, OHASH18000, ISO13485/FDA(OHC required) and quality tools.
f) Good Communication skills, self- discipline, problem solving oriented.
g) Good command of English both writing and spoken.
h) Good computer skill at MS-office., CAD, UG.
i) Good teamwork player.
职能类别: 产品工艺/制程工程师
公司介绍
荷兰皇家飞利浦公司是一家领先的健康科技公司,致力于在从健康生活方式、疾病预防、到诊断、治疗和家庭护理的整个“健康关护全程”,凭借先进的技术、丰富的临床经验和深刻的消费者洞察,不断推出整合的创新解决方案,助力健康医疗系统实现四重目标——提高大众健康水平、提高医护人员满意度、改善患者体验,并降低关护成本。飞利浦的愿景是通过有意义的创新,令世界更健康、更可持续的发展,到2030年每年改善25亿人的生活。
飞利浦公司总部位于荷兰,2021年销售额达172亿欧元,在全球拥有大约78,000名员工,销售和服务遍布世界100多个国家。公司目前在诊断影像、图像引导治疗、病人监护、医疗信息化以及消费者健康和家庭护理领域处于领导地位。
在飞利浦,每一个人,都至关重要。这是我们始终坚持的信念。在飞利浦,你将用数字化驱动有意义的创新,积极影响自己与数十亿人的生活,践行改善人类生活的使命。我们全心营造多元包容的工作环境,平等互助的工作氛围,让你的独特之处得到充分尊重和欣赏,鼓励你释放真我,以梦为马,不负韶华。本着 “立足中国,辐射全球” 的理念,我们通过布局广泛的业务线,为你带来广阔的平台、丰富的学习资源、多样的内部发展机会,助你成为具备全球化视野和本土深度的一专多能复合型稀缺人才。
创美好,做真我,迎蜕变。
我们深信每一个你都卓尔不凡, 更期待与志同道合的你笃行致远。
飞利浦公司总部位于荷兰,2021年销售额达172亿欧元,在全球拥有大约78,000名员工,销售和服务遍布世界100多个国家。公司目前在诊断影像、图像引导治疗、病人监护、医疗信息化以及消费者健康和家庭护理领域处于领导地位。
在飞利浦,每一个人,都至关重要。这是我们始终坚持的信念。在飞利浦,你将用数字化驱动有意义的创新,积极影响自己与数十亿人的生活,践行改善人类生活的使命。我们全心营造多元包容的工作环境,平等互助的工作氛围,让你的独特之处得到充分尊重和欣赏,鼓励你释放真我,以梦为马,不负韶华。本着 “立足中国,辐射全球” 的理念,我们通过布局广泛的业务线,为你带来广阔的平台、丰富的学习资源、多样的内部发展机会,助你成为具备全球化视野和本土深度的一专多能复合型稀缺人才。
创美好,做真我,迎蜕变。
我们深信每一个你都卓尔不凡, 更期待与志同道合的你笃行致远。
联系方式
- Email:ruby.chen@philips.com
- 公司地址:上海市静安区灵石路718号A1栋 (邮编:200233)
- 电话:13774217703