Supplier Quality Lead

Kenvue Inc.; Helsingborgs kommun; On-site; SEK 700,000 - 900,000; Full time

Job summary

Kenvue Inc.は、Helsingborg, SwedenにてSupplier Quality Leadを募集しています。この役割は、サプライヤーの品質管理戦略と基準の実装を担当し、サプライヤーとの連携を強化します。

候補者は科学的学士号を持ち、7～10年の業界経験と卓越したコミュニケーション能力が必要です。職場はフルオンサイトです。

Qualifications

• 7-10年の関連業界のビジネス経験.
• 品質管理または品質保証の現場経験はプラス.
• データに基づいた洞察と分析能力.

Responsibilities

• 直接資材サプライヤーのための品質ライフサイクル管理を担当.
• 規制要件および業界基準の遵守を確保.
• サプライヤーの信頼性を向上させるための戦略を開発.

Skills

コミュニケーション能力

分析力

問題解決能力

戦略的思考

Education

科学的学士号（薬学、化学、工学または関連分野）

Tools

品質管理システム

GMP

ISO 22716

Job description

Supplier Quality Lead

Kenvueは現在、以下求人を募集しております。

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。

Role reports to

EMEA Supplier Quality Lead

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

Role reports to: EMEA Supplier Quality Lead

Location: Helsingborg, Sweden

Travel %: up to 30%

What you will do

You will be responsible and accountable for the successful deployment, and implementation of the Supplier Quality Management (SQM) strategy and associated Kenvue quality standards, procedures, programs and initiatives that deliver quality/compliance, and value to Kenvue supply chain. Based on the Helsingborg site, you will actively partner with stakeholders, individuals and teams, and Direct Material (DM) suppliers to implement innovative solutions and continuous improvements with demonstrated and measurable business impact.

Key Responsibilities

• Own quality lifecycle management for Direct Material (DM) suppliers.
• Act as interface for the quality topics between the DM supplier and Kenvue.
• Ensure compliance with regulatory requirements and industry standards.
• Lead cross-functional teams to identify, develop and implement strategies to improve supplier reliability.
• Lead cross-functional supplier review governance meetings and supplier performance reviews with manufacturing sites.
• Establish close partnership with cross-functional team, Procurement, R&D, Raw Material Center, Global Packaging, Operations, to support Business growth and continuity, NPD, NPI & Cost improvement projects.
• Build strong partnership with Helsingborg Internal manufacturing site for leading investigation of the quality events, Supplier Event Notification (SEN), supporting material changes & participating in inspections/ audits.
• Build strong partnership with key suppliers and coordinate continuous improvement process at the suppliers through KPI, Management Action Plan, and CAPA.
• Own the audit planning for the assigned supplier ensuring timely execution of the audits.
• Drive key programs and initiatives across Quality & Compliance.
• Use data driven insights and analytics to identify trends, patterns, and opportunities for improvement across different areas.
• Drive performance management and be accountable for metrics, scorecards, and processes.
• Elaborate and present data insights and recommendations clearly to both technical and non-technical audiences, including senior management.

What we are looking for

Required Qualifications

• Scientific bachelor’s degree (Pharmacy, Chemistry, Engineering or related field). Master preferred.
• 7-10 years of relevant business experience in pharma/cosmetic/ chemical/ food/ packaging component industry. Field experience in Quality control or Quality assurance is a plus.
• Excellent communication, interpersonal, and influencing skills.
• Must be able to work independently and with others.
• Ability to think creatively and strategically to support business results.
• Strong analytical and problem-solving skills.
• Knowledge of regulatory requirements and industry standards.
• Fluent English.
• Hands on experience with Quality Management System, GMP, Agency compliance expectations, and ISO 22716.
• Good understanding of the European regulatory guidelines for drug Products
• Detailed understanding and application of current Good Manufacturing Practices and Agency compliance expectations

Desired Qualifications

• Ability to lead, teach, and guide project teams in using tools, initiating change, and applying sound process improvement methodology.
• Ability to manage budgets and resources effectively.
• Prior Supplier Quality management experience is a plus.

Kenvue is proud to be an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

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