Kenvueは現在、以下求人を募集しております。
QA Specialist (12 months)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:
Sr. Commercial Quality Specialist場所:
Asia Pacific, South Korea, Seoul, Seoul勤務地:
ハイブリッドあなたがすること
The responsibility of this job is to support the overall operation of Quality function ensuring compliance to Kenvue's global requirements and local regulations for GxP activities in Korea.
[Responsibilities]
Manage the quality inspection and test activities of imported OTC/Q- drug/Cosmetic products including incoming inspection of products and release testing.
Manage QA activities for imported OTC/Q- drug/Cosmetic products release from End to End, incoming inspection, sample shipment arrangement, release checklist preparation and so on.
Oversee the new product introduction process including test method transfer, QC tests, change control management and related documents preparation.
Implement the Quality System via transposition of the requirements of the Commercial Quality procedures.
Execute requirements regarding lifecycle management of GxP related documents and records (creation, approval, distribution, revision, retrieval, retention, disposition) to ensure regulatory compliance and business continuity.
Update and keep GxP documents up to date on EDMS.
Participate in the product performance related issue handling and product nonconformance with collaborating with cross functional quality teams.
Ensure appropriate Change control/Deviation/CAPA/Effectiveness check procedures are followed. Monitor quality records status for timely closure and support issues using QMS.
Ensure a review of the APQRs as required by local regulations.
Support product complaint management.
Support internal audit and HA inspection for auditing and documentation
Support supplier qualification and document management.
What we are looking for
[Requirements]
- Bachelor’s degree or equivalent / Science, Chemistry, Biology, Biochemistry, etc.
- At least 2-4 years of experience preferred in the Pharmaceutical or related industry, ideally with QA & QC operations.
- Fluency in English and Korean (spoken and written)
障害のある個人の方は、宿泊施設のリクエスト方法について障害支援ページを確認してください。
