Kenvueは現在、以下求人を募集しております。
Quality Excellence Lead私たちがしていること
私たちKenvueは、日々のケアが持つ驚くべき力を信じています。100年以上の伝統と科学に根ざし、Neutrogena®, Aveeno®, Tylenol®, Listerine®, Johnson’s® and BAND-AID®など、皆様が既にご存じでご愛用いただいているアイコニックなブランドを提供しています。科学は私たちの情熱であり、ケアは私たちの才能です。
Who We Are
私たちのグローバルチームは、インサイトとイノベーションに情熱を注ぎ、最高の製品をお客様にお届けすることに全力を注ぐ、多様で優秀な22,000人以上の社員で構成されています。専門知識と共感力を備えたKenvuerであることは、毎日何百万人もの人々の生活に影響を与える力を持つことを意味します。私たちは、人を第一に考え、全身全霊をもってケアし、サイエンスで信頼を獲得し、勇気をもって解決します。私たちとあなた自身の未来を、共に切り開いていきましょう。
Role reports to:
APAC Strategic Program Management Lead場所:
Asia Pacific, Thailand, Bangkok, Bangkok勤務地:
フルオンサイトあなたがすること
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® Brand Adhesive Bandages that you already know and love. Science is our passion; care is our talent. Our global team is made up of ~ 22,000 diverse and brilliant people, passionate about insights, innovation and committed to delivering the best products to our customers. With expertise and empathy, being a Kenvuer means having the power to impact the 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 Excellence Associate Manager under Asia Pacific Quality & Compliance Strategic Program Management organization is responsible for consolidating and executing quality initiatives as well as supporting talent capability building agenda for APAC. This is also a cross-functional facing role for Quality function to ensure a deep understanding of compliance standards and operational excellence to ensure all initiatives are assess, coordinated, and seamlessly deliver against organizational goals.
Key Responsibilities
- Responsible for coordinating and executing Quality function core programs and initiatives from intake assessment, resource planning, facilitating solution exploration, deployment and change management. In areas such as manufacturing and market quality, laboratories operations, supplier quality and quality systems.
- Participate and contribute as subject matter expert of applicable Global Quality workstreams and support execution of pillars’ activities and driving quality culture, capabilities, and development for the region.
- Partner with business process owners to define the project scope, objectives, and deliverables. And convert into comprehensive project plans and schedules, including setting deadlines, communicating responsibilities, and monitoring progress.
- Support identify and manage project dependencies and critical paths and manage changes in project scope, identify potential crises, and devise contingency plans.
- Coordinate to develop and deliver progress reports, proposals, requirements documentation, and presentations and communicate with cross-functional regional teams to facilitate seamless project execution and resolve any issues that may arise.
- Provide roll out training to Sites’ users, which includes quality project portfolio management tools, application quality system platforms, laboratory information management system, enterprise resource planning system.
Qualifications
- Bachelor’s degree in Science, Engineering, or equivalent field with extensive and relevant business experience in project portfolio management.
- A minimum of 5 years of experience in quality management of Good Manufacturing Practices of regulated environment, either in Consumer Health, Pharmaceutical, Medical Device, and/or Food and Dietary Supplements industry.
- This role requires a diverse quality background, preferably with hands-on experience in multiple quality disciplines in manufacturing quality, commercial quality, laboratory operation, quality systems.
- Strong understanding of quality system tools, systems & processes, laboratory information management system, enterprise resource planning system and computerized system validation
- Hand-on experience in project management and capable of managing multiple projects and initiatives.
- Knowledge in process improvement such as LEAN, Kaizen, Six-sigma, Statical Process Control, data analytics with digital tools.
- High problem solving & continues improvement, ability to coach team for assessment and explore innovative resolution which includes advance laboratory technology, digitalization, and processes improvement.
- Outstanding interpersonal capabilities, experience with collaborating, networking, with all levels of management and lead discussions without line authority to create alignment of senior cross-functional team members, and ability to function as a change agent and adapt to changing business dynamics is required.
- Excellent communication, proficiency in English, both verbal and written and facilitation skills promote collaboration with physical and virtual groups are essential.
Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, protected veteran status, or any other legally protected characteristic, and will not be discriminated against on the basis of disability.
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