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我們做什麼
在 Kenvue，我們意識到日常護理的非凡力量。我們以一個多世紀的傳統為基礎，植根於科學，是標誌性品牌的品牌 - 包括您已經熟悉和喜愛的 NEUTRGENA®、AVEENO、TYLENOL®®、LISTERINE®、JOHNSON'S® 和 BAND-AID®。科學是我們的熱情所在;關心就是我們的才能。
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我們的全球團隊由 ~ 22,000 名才華橫溢的員工組成，他們的職場文化中，每個聲音都很重要，每一個貢獻都受到讚賞。 我們熱衷於洞察， 創新並致力於為我們的客戶提供最好的產品。憑藉專業知識和同理心，成為 Kenvuer 意味著每天有能力影響數百萬人。我們以人為本，熱切關懷，以科學贏得信任，以勇氣解決——有絕佳的機會等著您！加入我們，塑造我們和您的未來。有關更多資訊，請按兩下 here.
Role reports to：
GER QA E CONFORM SR位置：
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos工作地點：
混合你會做什麼
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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