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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：
Sr. Commercial Quality Specialist位置：
Asia Pacific, South Korea, Seoul, Seoul工作地點：
混合你會做什麼
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)
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