Kenvue 目前正在招聘 a：
我们做什么
在 Kenvue，我们意识到日常护理的非凡力量。我们以一个多世纪的传统为基础，植根于科学，是标志性品牌的品牌 - 包括您已经熟悉和喜爱的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科学是我们的热情所在;关心就是我们的才能。
我们是谁
我们的全球团队由 ~ 22,000 名才华横溢的员工组成，他们的职场文化中，每个声音都很重要，每一个贡献都受到赞赏。 我们热衷于洞察， 创新并致力于为我们的客户提供最好的产品。凭借专业知识和同理心，成为 Kenvuer 意味着每天有能力影响数百万人。我们以人为本，热切关怀，以科学赢得信任，以勇气解决——有绝佳的机会等着您！加入我们，塑造我们和您的未来。有关更多信息，请单击 here.
Role reports to：
GER QA E CONFORM SR位置：
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos工作地点：
混合你会做什么
Kenvue is currently recruiting for:
Project Site Lead (Quality Control) - Fixed Term (12 months)
This position reports into Quality structure based at Kenvue SJC, BRAZIL site.
Who We Are
At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we’re the house of iconic brands - including NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON’S® and BAND-AID® that you already know and love. Science is our passion; care is our talent. Our global team is made by 22,000 diverse and brilliant people, passionate about insights, innovation and committed to deliver the best products to our customers. With expertise and empathy, being a Kenvuer means to have the power to impact life of millions of people every day. We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information click here.
What You Will Do
The Quality Control Sr Analyst will be responsible for Project management and implementation of Quality Laboratories of the Future Program, reporting to Regional Quality project manager. This role will be responsible for delivering quality plans across the SJC laboratories in order to achieve project milestones in several workstreams such as lims implementation, system new functionalities integrations, equipment lifecycle management, equipment automation and connectivity, test method optimization, change management, documentation updates including change control coordination and others.
Key Responsibilities
- LIMS New functionalities Project, acting as focal point in the labs and with global stakeholders
- Project Team management
- Equipment integration (with LIMS)
- Change Management
- Risk Management
- Facilitate trainings
- Interface with IT and suppliers
- Lab Processes Improvement
What We Are Looking For
Required Qualifications
- Bachelor's degree in pharmacy, chemical engineering, chemistry or equivalent technical field required
- A minimum of 5 years of relevant professional work experience in the field regulated health industry : Cosmetic/Device/Drug regulated environment
- Solid Experience in Laboratories
- Proven experience in leading virtual within dynamic settings in a regional /cross-functional environment.
- Project management certification is preferred
- Solid technical (quality/regulatory) knowledge
- Understanding of LATAM GxP regulations applicable for cosmetics, devices, pharmaceutical industries.,
Desired Qualifications /Technical competences
- Ability to lead and motivate teams
- Excellent problem-solving and conflict resolution skills
- Consistent track record to work cross-functionally
- Flexibility and adaptability to thrive in a multifaceted environment
- Attention to detail and a drive for ensuring data accuracy and integrity
- Strong demonstrated collaboration, sense of urgency, analytical, influencing skills
- Understanding of project controls and scheduling
- Must be able to develop and maintain relationships/partnerships and to work collaboratively
- Advanced English
- Advanced Spanish
What’s In It For You
- Competitive Benefit Package
- Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More!
- Learning & Development Opportunities
- Employee Resource Groups
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.
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