Kenvueは現在、以下求人を募集しております。
Analista Sênior de Qualidade – Reclamações e Vigilância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:
Director Global Complaint Vigilance場所:
Latin America, Brazil, Sao Paulo, Sao Jose dos Campos勤務地:
ハイブリッドあなたがすること
Atualmente estamos com 4 posições abertas para Analista Senior.
The SR COMPLAINT VIGILANCE ANALYST is responsible for processing product quality complaints and supporting day-to-day activities for complaint management for the North America region and globally (as needed) including but not limited to:
Key Responsibilities
- Evaluate complaints in alignment with the product quality complaint program. This may include, but is not limited to, trend analysis, assignment of complaint to manufacturing site, review of manufacturing site investigation, complaint closure as applicable, and escalation as needed.
- Review and process updated information for complaint change logs from the call center and medical safety to assess impact on triage and investigation process.
- Collaborate with cross-functional teams such as Global Consumer Care, Medical Safety Internal affiliates and External site representatives to address and resolve complaints efficiently.
- Complete Annual Drug Product Review contributions, Complaint Vigilance reports, and presentations per established procedures. Prepare and issue meeting minutes and ensure action items are complete.
- Assist with/participates in various projects and activities related to Complaint Vigilance processes, system implementations, and improvements.
- Monitor Complaint Records in the complaint management system to ensure standard processes are being followed and complaints are closed as required.
- Compile product and lot-specific complaint trending data and complaint closure metrics as requested.
- Support internal and external audits and inspections as a Subject Matter Expert as needed.
- Provide training and guidance to junior analysts on complaint vigilance processes and procedures.
- As necessary, this position will support the Analyst functions in other Geographical regions for Consumer products.
Required Qualifications
- Bachelor’s Degree in Science/Engineering or a related discipline
- Minimum 5 years of related experience in Quality Assurance and/or complaint management in pharmaceutical, medical device, nutritional or related industry experience
- Detail-oriented with the ability to document and track corrective actions and complaint investigations.
- Knowledge of regulatory requirements and quality assurance processes in the healthcare industry
- Proficiency in the use of computer systems and applications such as Microsoft Office Suite
- Strong analytical skills with the ability to interpret complex data and identify trends.
- Ability to work independently and prioritize tasks in a fast-paced environment.
- Language Requirement: Both Portuguese and English (effectively writing & speaking)
Desired Qualifications
- Excellent communication and interpersonal skills to effectively collaborate with internal and external stakeholders.
- Problem-solving abilities and focus on accuracy and precision in data analysis and reporting.
- Advanced skills in PowerPoint and Excel include v-look up, H look-up, macros, and pivot tables.
- Experience supporting manufacturing, packaging, and development operations.
- Experience with complaint handling software applications.
- Experience with systems and tools supporting analysis and reporting including Power BI, Tableau.
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。
