Supplier Quality Lead

McNeil; Helsingborgs kommun; On-site; SEK 669,600 - 948,600; Full time

Job summary

Kenvue is seeking a Supplier Quality Lead based in Helsingborg, Sweden, responsible for executing and implementing the Supplier Quality Management strategy. This role demands strong partnerships with suppliers and cross-functional teams to ensure compliance and drive improvements.

Applicants should possess a scientific degree and 7-10 years of experience in the relevant industry. Excellent communication and analytical skills are a must. The position is fully onsite.

Qualifications

• 7-10 years of relevant business experience in pharma/cosmetic/chemical/food/packaging.
• Field experience in Quality Control or Assurance is a plus.
• Hands-on experience with ISO 22716.

Responsibilities

• Own quality lifecycle management for Direct Material suppliers.
• Lead cross-functional teams to improve supplier reliability.
• Drive key programs and initiatives across Quality & Compliance.

Skills

Communication skills

Analytical skills

Problem-solving skills

Regulatory knowledge

Education

Scientific bachelor's degree (Pharmacy, Chemistry, Engineering)

Master's degree preferred

Tools

Quality Management System

GMP

Job description

Kommun: Helsingborg

Kenvue is currently recruiting for a: Supplier Quality Lead

Role reports to: EMEA Supplier Quality Lead

Work Location: Fully Onsite

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.
• 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.