Supplier Quality Lead

Supplier Quality Lead

Ce que nous faisons

Chez Kenvue, nous réalisons le pouvoir extraordinaire des soins quotidiens. S'appuyant sur plus d'un siècle d'héritage et enraciné dans la science, nous sommes la maison de marques emblématiques - dont NEUTROGENA®, AVEENO®, TYLENOL®, LISTERINE®, JOHNSON'S® et BAND-AID® que vous connaissez et aimez déjà. La science est notre passion ; Le soin est notre talent.

Qui nous sommes

Notre équipe mondiale est composée de ~ 22 000 personnes brillantes avec une culture d'entreprise où chaque voix compte et chaque contribution est appréciée. Nous sommes passionnés par les idées, l'innovation et l'engagement à fournir les meilleurs produits à nos clients. Avec de l'expertise et de l'empathie, être un Kenvuer signifie avoir le pouvoir d'avoir un impact sur des millions de personnes chaque jour. Nous donnons la priorité aux personnes, nous nous soucions farouchement, nous gagnons la confiance grâce à la science et nous résolvons les problèmes avec courage - et nous vous offrons de brillantes opportunités ! Joignez-vous à nous pour façonner notre avenir et le vôtre. Pour plus d'informations, cliquez sur ici.

Role relève à :

EMEA Supplier Quality Lead

Lieu :

Europe/Middle East/Africa, Sweden, Skane, Helsingborg

Lieu de travail :

Entièrement sur place

Ce que tu vas faire

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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