Kenvue 目前正在招聘 a:
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。
我們是誰
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:
Resp Qualite compliance é systemes de laboratoire senior位置:
Europe/Middle East/Africa, Switzerland, Zug, Rotkreuz工作地點:
混合你會做什麼
Quality Vigilance and Rapid Response Manager
Summary
Kenvue is currently recruiting for a Quality Vigilance and Rapid Response Manager for EMEA internal manufacturing sites.
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.
Job purpose
The Quality Vigilance and Rapid response Manager is the regional contact for quality issues, and proactive & continuous improvement initiative compliance related to impacting EMEA internal manufacturing sites. This individual is responsible for supporting Quality issue Lifecycle management, advising on resolution and supporting continuous improvement in close collaboration with R&D.
Major duties & responsibilities
Partner with R&D and supply chain to coordinate and support complex quality issues towards resolution while ensuring root cause elimination. List non exhaustive of complex issue is significant escalation, Non-conformance impacting multiple sites, supply disruption
Interacts with cross-functional teams especially R&D, supply chain and Make Q&C to ensure excellence in execution
Prepare, and document significant escalation
Prepares and facilitate the Filed actions Board
Create and support communication to quality and Business for the scope of responsibility
Centralize, and support compliance portfolio impacting internal manufacturing sites Quality representative for R&D and supply chain value stream projects governance
Orchestrate key compliance initiatives for IM sites
Manage project as per assignment
Consolidates and oversees related performance management consolidates Quality Issues from the different sources (Complaints, Non-Conformances etc…) support resolution, perform trend analysis
Seeks, uncovers and integrates new opportunities into performance management providing support towards continuous improvement. - (i.e Corrective, Preventive actions and Proactive initiatives)
Input regional performance, and Quality Management Review
undefined
Ensures compliance with relevant industry standards and regulations
Qualifications
A bachelor’s degree or equivalent in chemical/physical sciences, Business or a related discipline.
A minimum of 8 years of relevant business experience and a minimum of 5 years of responsibility in quality & compliance in consumer and/or pharmaceutical industries.
Fluent in English (spoken and written)
Strong leadership, project management and performance skills
Ability to handle high-pressure situations and make informed decisions quickly
Excellent communication and interpersonal skills
Strong problem-solving and troubleshooting abilities
Demonstrated leadership & influencing skills across organizational levels
Detail-oriented with a strong focus on quality and continuous improvement
Demonstrated company-wide knowledge and experience leading cross-functional teams
Strong Business Acumen
Other:
This position will be based in Prague/Rotkreuz /Germany/Sweden and may require up to 20% domestic travel
Hiring Manager: Magali Olivie
PG 30
如果您是殘障人士,請查看我們的 殘障人士援助頁面瞭解如何申請便利