Senior Product Engineer
青岛伦敦杜蕾斯有限公司
- 公司规模:1000-5000人
- 公司性质:外资(欧美)
- 公司行业:快速消费品(食品、饮料、化妆品)
职位信息
- 发布日期:2013-07-04
- 工作地点:青岛
- 招聘人数:1
- 工作经验:五年以上
- 学历要求:本科
- 语言要求:英语熟练
- 职位类别:产品工艺/制程工程师 项目工程师
职位描述
SUMMARY:
This R&D role is the critical link between Category R&D and Supply, providing ongoing product support to Supply. The group leads development activities in the medium to long term to resolve production issues, implementation of product enhancements, and defence of net revenue.
PROFESSIONAL QUALIFICATIONS / EXPERIENCE:
-A Bachelors degree minimum in a relevant science, supplemented by direct work experience in latex and/or medical device industry and/or familiarity with Reckitt Benckiser practices and procedures where possible
-IT skills required include
oProficiency in the Microsoft Suite of programs: Word, Excel, Powerpoint, Outlook
oAbility to quickly learn to navigate other software programs required to execute workplace activities
SCOPE / DIMENSIONS OF ROLE:
The role will have involvement in all formulation and process related changes to natural and synthetic rubber condoms production. This includes the span from second source/replacement raw material evaluations through process/product qualification exercises.
The role may also include management of one or more direct reports
RESPONSIBILITIES / ACCOUNTABILITIES:
General :
?To ensure that any major changes to the condom manufacturing process are validated and comply with the appropriate company guidelines and regulations. The scope of works include the following
oNew or significantly modified production process (in conjunction with R&D where appropriate)
oNew production machine design or major modification (Major change)
oNew Condom Shape/ Type
oDevelop and implement medium to long term issue resolutions
?To ensure that raw material changes are validated and comply with the appropriate company guidelines and regulations. The scope of works are as the following
oRaw Material related to Latex Compounding Formulation (Latex, Chemical, Pigment)
oRaw Material related to Compound Dispersion
oRaw Material related to Finishing Material
oRaw Material related to Lubricant Formulation
?To support the standardization projects between the Thailand and China sites
?To support the Production troubleshooting and regulatory requirements where required/ appropriate.
?To update specifications, SOP’s, Product Safety Data Sheets, and other related documents
?To serve as a technical liaison to Regulatory Affairs in answering customer inquiries and resolving customer complaints.
?To provide technical support for New Product Development projects where required/ appropriate.
?To support cost savings projects where required/ appropriate.
?To manage the product validation protocols & reports, execute and updated stability studies and report as scheduled.
?To maintain/organize all validation works document in Process Development area.
?To carry out other works as assigned by the ESG Latex Manager.
Quality :
?Be aware, accountable and follow GMP (Good Manufacturing Practice) rules & regulations
?Enforce quality mind by ‘Right first time’ practice for working in area by following documented procedures & follow good documentation practice
Safety, Health & Environment :
?Be aware, accountable for safety, health & environment in workplace all time to ensure free-accident & good environment area of working
?Follow safety, health & environment regulations & policy by working safely, reporting unsafe condition / unsafe act / near miss accident to supervisor as well as suggest for any improvement
This R&D role is the critical link between Category R&D and Supply, providing ongoing product support to Supply. The group leads development activities in the medium to long term to resolve production issues, implementation of product enhancements, and defence of net revenue.
PROFESSIONAL QUALIFICATIONS / EXPERIENCE:
-A Bachelors degree minimum in a relevant science, supplemented by direct work experience in latex and/or medical device industry and/or familiarity with Reckitt Benckiser practices and procedures where possible
-IT skills required include
oProficiency in the Microsoft Suite of programs: Word, Excel, Powerpoint, Outlook
oAbility to quickly learn to navigate other software programs required to execute workplace activities
SCOPE / DIMENSIONS OF ROLE:
The role will have involvement in all formulation and process related changes to natural and synthetic rubber condoms production. This includes the span from second source/replacement raw material evaluations through process/product qualification exercises.
The role may also include management of one or more direct reports
RESPONSIBILITIES / ACCOUNTABILITIES:
General :
?To ensure that any major changes to the condom manufacturing process are validated and comply with the appropriate company guidelines and regulations. The scope of works include the following
oNew or significantly modified production process (in conjunction with R&D where appropriate)
oNew production machine design or major modification (Major change)
oNew Condom Shape/ Type
oDevelop and implement medium to long term issue resolutions
?To ensure that raw material changes are validated and comply with the appropriate company guidelines and regulations. The scope of works are as the following
oRaw Material related to Latex Compounding Formulation (Latex, Chemical, Pigment)
oRaw Material related to Compound Dispersion
oRaw Material related to Finishing Material
oRaw Material related to Lubricant Formulation
?To support the standardization projects between the Thailand and China sites
?To support the Production troubleshooting and regulatory requirements where required/ appropriate.
?To update specifications, SOP’s, Product Safety Data Sheets, and other related documents
?To serve as a technical liaison to Regulatory Affairs in answering customer inquiries and resolving customer complaints.
?To provide technical support for New Product Development projects where required/ appropriate.
?To support cost savings projects where required/ appropriate.
?To manage the product validation protocols & reports, execute and updated stability studies and report as scheduled.
?To maintain/organize all validation works document in Process Development area.
?To carry out other works as assigned by the ESG Latex Manager.
Quality :
?Be aware, accountable and follow GMP (Good Manufacturing Practice) rules & regulations
?Enforce quality mind by ‘Right first time’ practice for working in area by following documented procedures & follow good documentation practice
Safety, Health & Environment :
?Be aware, accountable for safety, health & environment in workplace all time to ensure free-accident & good environment area of working
?Follow safety, health & environment regulations & policy by working safely, reporting unsafe condition / unsafe act / near miss accident to supervisor as well as suggest for any improvement
公司介绍
利洁时是一家使命担当和奋斗目标驱动的企业,我们的使命是“通过卫生防护,健康疗护,营养守护,竭力创造更洁净、更健康的世界”;在这一使命指引下,我们的奋斗目标是“让人们平等地享有高品质的卫生、健康和营养”。
利洁时旗下拥有众多深受消费者信赖的知名品牌,涵盖卫生、健康和营养三大品类,其中包括美赞臣旗下各品牌(蓝臻/Enfinitas、铂睿/Enfamil、安儿宝Enfagrow、亲舒/Gentlease、安敏健/Nutramigen、学优力/NutriPower、致沛)、诺洛芬/Nurofen、使立消/Strepsils、嘉胃斯康/Gaviscon、美清痰/Mucinex、杜蕾斯/Durex、Clearasil、乐守/Lysol、滴露/Dettol、薇婷/Veet、亮湃/Harpic、Cillit Bang、Mortein、亮碟/Finish、渍无踪/Vanish、Calgon、护丽/Woolite、Air Wick等。
全球消费者平均每天购买2,000万件利洁时产品。利洁时始终满怀热诚地持守以下准则:消费者优先、以人为本;坚持探索新机、寻求发展;坚持打造成功、共享共赢;坚持精益求精、追求卓越。我们终坚持做正确的事。
利洁时在世界各地有43,000多位来自不同文化、才华横溢的员工。我们正在共同努力,为实现公司使命、创造更洁净的世界、成就更平等的社会不断奋进前行。
利洁时在广州、北京、上海、厦门分别设有主要办公室;在山东青岛、湖北荆州、安徽马鞍山、广东广州设有4家工厂;在山东青岛、湖北沙市、安徽马鞍山、广东东莞、广东广州设有5大研发实验室,在东莞设有东亚采购中心(EAST),销售网络遍及整个中国。
关于青岛伦敦杜蕾斯
青岛伦敦杜蕾斯有限公司是目前世界级的安全套生产基地之一,于1998年作为合资公司进入中国。2007年,SSL集团买断中方的股份,成为独资公司。2010年,伴随着SSL集团被利洁时收购,青岛伦敦杜蕾斯公司成为利洁时集团属下的全资子公司。
公司现有一千多名员工,截至到2016年5月共有生产线31条,产品销往中国、比利时、加拿大、德国、希腊、英国、中东、荷兰、波兰、俄罗斯、澳大利亚、尼日利亚、新西兰、美国、加拿大等20多个国家和地区。
公司已经获得:ISO9001质量管理体系认证、ISO13485医疗器械质量管理体系认证、ISO14001环境体系认证、OSHAS18001职业健康安全体系认证、英国风筝标志和欧盟CE标志、法国LNE认证、南非SABS认证、韩国FDA认证、美国FDA认证、德国DLF认证等证书。
利洁时旗下拥有众多深受消费者信赖的知名品牌,涵盖卫生、健康和营养三大品类,其中包括美赞臣旗下各品牌(蓝臻/Enfinitas、铂睿/Enfamil、安儿宝Enfagrow、亲舒/Gentlease、安敏健/Nutramigen、学优力/NutriPower、致沛)、诺洛芬/Nurofen、使立消/Strepsils、嘉胃斯康/Gaviscon、美清痰/Mucinex、杜蕾斯/Durex、Clearasil、乐守/Lysol、滴露/Dettol、薇婷/Veet、亮湃/Harpic、Cillit Bang、Mortein、亮碟/Finish、渍无踪/Vanish、Calgon、护丽/Woolite、Air Wick等。
全球消费者平均每天购买2,000万件利洁时产品。利洁时始终满怀热诚地持守以下准则:消费者优先、以人为本;坚持探索新机、寻求发展;坚持打造成功、共享共赢;坚持精益求精、追求卓越。我们终坚持做正确的事。
利洁时在世界各地有43,000多位来自不同文化、才华横溢的员工。我们正在共同努力,为实现公司使命、创造更洁净的世界、成就更平等的社会不断奋进前行。
利洁时在广州、北京、上海、厦门分别设有主要办公室;在山东青岛、湖北荆州、安徽马鞍山、广东广州设有4家工厂;在山东青岛、湖北沙市、安徽马鞍山、广东东莞、广东广州设有5大研发实验室,在东莞设有东亚采购中心(EAST),销售网络遍及整个中国。
关于青岛伦敦杜蕾斯
青岛伦敦杜蕾斯有限公司是目前世界级的安全套生产基地之一,于1998年作为合资公司进入中国。2007年,SSL集团买断中方的股份,成为独资公司。2010年,伴随着SSL集团被利洁时收购,青岛伦敦杜蕾斯公司成为利洁时集团属下的全资子公司。
公司现有一千多名员工,截至到2016年5月共有生产线31条,产品销往中国、比利时、加拿大、德国、希腊、英国、中东、荷兰、波兰、俄罗斯、澳大利亚、尼日利亚、新西兰、美国、加拿大等20多个国家和地区。
公司已经获得:ISO9001质量管理体系认证、ISO13485医疗器械质量管理体系认证、ISO14001环境体系认证、OSHAS18001职业健康安全体系认证、英国风筝标志和欧盟CE标志、法国LNE认证、南非SABS认证、韩国FDA认证、美国FDA认证、德国DLF认证等证书。
联系方式
- 公司地址:地址:span青岛市城阳区青岛高新区岙东路上马段1-13号