Kenvueは現在、以下求人を募集しております。
Auditor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:
Quality System & Performance Manager場所:
Europe/Middle East/Africa, Sweden, Skane, Helsingborg勤務地:
フルオンサイトあなたがすること
The Auditor is responsible for keeping quality records up to date, managing change control activities, and supporting corrective action plans. You will investigate issues, review data trends, support audits, and suggest improvements to strengthen quality systems and ensure inspection readiness.
**Key Responsibilities**
Create and apply audit approaches using data and risk analysis to identify potential issues early and improve audit planning.
Lead audits that involve different teams and use new tools or technologies to improve compliance, visibility, and quality systems.
Develop and update audit and quality frameworks to meet changing regulations, business needs, and process requirements.
Work closely with business teams to identify quality issues and suggest effective corrective and preventive actions.
Maintain clear, accurate, and timely quality and audit records.
Manage change control documentation and approval processes to ensure compliance, traceability, and proper implementation of corrective actions.
Review existing audit and quality systems, recommend improvements to increase compliance and efficiency, and help implement approved changes.
Prepare for and support internal and external audits and inspections to ensure ongoing inspection readiness.
Assist in creating, updating, and reviewing standard operating procedures, especially those involving suppliers and audits.
Support special quality and audit projects across different functions to ensure continuous improvement and regulatory compliance.
What we are looking for
**Required Qualifications**
Master’s degree or equivalent in Engineering, Biomedicine, Pharmacy or a related field.
Experience in auditing, quality assurance, in a regulated environment.
Strong understanding of quality management systems, CAPA processes, and regulatory requirements.
Experience managing documentation, performing investigations, analyzing data, and preparing quality reports.
Experience supporting audits and inspections with a focus on inspection readiness.
Strong communication and collaboration skills to work effectively with different teams and external partners.
Strong attention to detail, good organization skills, and the ability to manage multiple tasks in a fast-paced environment.
Fluent in both Swedish and English
**Desired Qualifications**
Strong analytical and problem-solving skills.
Experience using data analytics tools and audit software to improve audit effectiveness.
Strong communication skills with experience influencing stakeholders and leading audit activities.
Ability to adapt to changing regulations and a strong interest in continuous learning and development.
Experience reviewing processes, improving quality systems, and implementing corrective actions.
Experience using quality management systems and tools for documentation and process support.
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