Quality Assurance Specialist 6 month contract
丝芙兰（上海）化妆品销售有限公司
- 公司性质：合资(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：2016-11-14
- 工作地点：上海-静安区
- 招聘人数：1人
- 工作经验：3-4年经验
- 学历要求：本科
- 语言要求：英语 良好
- 职位月薪：10000-14999/月
- 职位类别：质量检验员/测试员 审核员
职位描述
职位描述：
Duties and Responsibilities:
1. New project development
- Risk analysis for Quality part.
- Define test plan for pilot batch (e.g. stability, compatibility, packaging test, etc.), coordinate the test with supplier and 3rd party lab, chase for test reports and timely update the test results with team.
- Conduct pilot batch production and line trial if required for key project.
- Quality check for bulk submission and finished goods with proper record.
- Chasing and review all the quality declaration, deliverables files with supplier during development.
2. Tag on project support
- Quality check for bulk submission and finished goods with proper record.
- Chasing and review all the quality declaration, deliverables files with supplier during development.
3. Reorder QA
- Quality check for bulk submission and finished goods with proper record.
- Qualification check updates with existing suppliers.
4. Audit
- Define and update annual audit plan (quality, social, environmental)
- Coordinate and ensure audit to be conducted by 3rd party agency by annual plan.
- Chasing for audit report with agency and action plan follow up with suppliers.
- Quarterly updating the audit results to S+ FR HQ.
5. Budget Control
- Define annual test budget.
- Apply PO& payment for all the test and audit.
- Monthly review & timely accrual with proper control.
Qualifications:
- Chemistry related majors related in healthcare, cosmetics.
- Min. 2 years’ experience in QC (analytics)
- Min. 2 years’ experience in QA (auditing)
- Min. 3 years working experience in pharmaceutical/cosmetics company, or 3rd party test lab laboratory.
- Fluent English spoken and written is a must.
- "Rules" oriented, detail oriented and deadline driven.
- Knows and acts according to the quality standard/principles, in particular LVMH standard.
- Speaks up when any of these principles are violated or compromised.
- "Rules" oriented, to OWN our regulatory rules, to efficiently impose our strict rules to our suppliers, to follow up with them daily, in order to make sure all our products are up to our Group standards
- Detail oriented, to make sure every detail of the our product is 100% compliant
- With good communication skills, to ensure very clear info sharing across related departments (S+ FR regulatory team, China RCA team, China supply chain, suppliers, etc.)
- Well-organized, with strong logic thinking and very good deadline management.
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Duties and Responsibilities:
1. New project development
- Risk analysis for Quality part.
- Define test plan for pilot batch (e.g. stability, compatibility, packaging test, etc.), coordinate the test with supplier and 3rd party lab, chase for test reports and timely update the test results with team.
- Conduct pilot batch production and line trial if required for key project.
- Quality check for bulk submission and finished goods with proper record.
- Chasing and review all the quality declaration, deliverables files with supplier during development.
2. Tag on project support
- Quality check for bulk submission and finished goods with proper record.
- Chasing and review all the quality declaration, deliverables files with supplier during development.
3. Reorder QA
- Quality check for bulk submission and finished goods with proper record.
- Qualification check updates with existing suppliers.
4. Audit
- Define and update annual audit plan (quality, social, environmental)
- Coordinate and ensure audit to be conducted by 3rd party agency by annual plan.
- Chasing for audit report with agency and action plan follow up with suppliers.
- Quarterly updating the audit results to S+ FR HQ.
5. Budget Control
- Define annual test budget.
- Apply PO& payment for all the test and audit.
- Monthly review & timely accrual with proper control.
Qualifications:
- Chemistry related majors related in healthcare, cosmetics.
- Min. 2 years’ experience in QC (analytics)
- Min. 2 years’ experience in QA (auditing)
- Min. 3 years working experience in pharmaceutical/cosmetics company, or 3rd party test lab laboratory.
- Fluent English spoken and written is a must.
- "Rules" oriented, detail oriented and deadline driven.
- Knows and acts according to the quality standard/principles, in particular LVMH standard.
- Speaks up when any of these principles are violated or compromised.
- "Rules" oriented, to OWN our regulatory rules, to efficiently impose our strict rules to our suppliers, to follow up with them daily, in order to make sure all our products are up to our Group standards
- Detail oriented, to make sure every detail of the our product is 100% compliant
- With good communication skills, to ensure very clear info sharing across related departments (S+ FR regulatory team, China RCA team, China supply chain, suppliers, etc.)
- Well-organized, with strong logic thinking and very good deadline management.
职能类别： 质量检验员/测试员 审核员
关键字： Quality control QA
公司介绍
丝芙兰--备受全球消费者挚爱的美力社区，始终致力于为消费者及品牌提供最独特的零售体验，鼓励他们自由大胆地探索及创造自我美力。
1969年，丝芙兰由多米尼克？曼东诺德(Dominique Mandonnaud)在法国创立，带来突破及创新的品牌理念，与一众品牌伙伴建立了紧密的合作关系——经典大牌、独立小众品牌、新晋潮流品牌以及好评如潮的丝芙兰自有品牌组成美妆矩阵，为消费者提供多元选择，引领消费者感知姿态万千的美力世界。
全球高端美妆零售商，于1997年加入全球奢侈品巨头 – 法国路威酩轩集团Moet Hennessy – Louis Vuitton(以下简称LVMH). LVMH旗下拥有近70个各具特色的著名品牌。集团主要业务包括葡萄酒和烈酒、时装和皮革制品、香水和化妆品、钟表和珠宝及精品零售五个领域。品牌包括酩悦香槟，路易威登，思琳，迪奥，斐登，真力时和泰格豪雅等等。
1969年，丝芙兰由多米尼克？曼东诺德(Dominique Mandonnaud)在法国创立，带来突破及创新的品牌理念，与一众品牌伙伴建立了紧密的合作关系——经典大牌、独立小众品牌、新晋潮流品牌以及好评如潮的丝芙兰自有品牌组成美妆矩阵，为消费者提供多元选择，引领消费者感知姿态万千的美力世界。
全球高端美妆零售商，于1997年加入全球奢侈品巨头 – 法国路威酩轩集团Moet Hennessy – Louis Vuitton(以下简称LVMH). LVMH旗下拥有近70个各具特色的著名品牌。集团主要业务包括葡萄酒和烈酒、时装和皮革制品、香水和化妆品、钟表和珠宝及精品零售五个领域。品牌包括酩悦香槟，路易威登，思琳，迪奥，斐登，真力时和泰格豪雅等等。