Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We create products and solutions that help advance industries by providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, promote sustainability, circularity, and transparency, and connect brands and consumers more effectively. Our offerings include labeling and functional materials, RFID inlays and tags, software applications that connect the physical and digital worlds, and enhanced branded packaging that improves customer experience. Serving industries worldwide—including home and personal care, apparel, retail, e-commerce, logistics, food and grocery, pharmaceuticals, and automotive—we employ approximately 35,000 employees across more than 50 countries. Our reported sales in 2024 were $8.8 billion. Learn more at www.averydennison.com.
Avery Dennison is an equal opportunity employer.
Please inform us if we can support you with reasonable accommodations throughout the application process by contacting our team via Requestaccomodation@eu.averydennison.com.
We do not accept unsolicited referrals or resumes from any source other than directly from candidates.
*We are unable to offer sponsorship or relocation for this role.*
*This role is subject to right-to-work checks as per local employment laws.*
Job Description
The successful candidate will be part of an established Quality team and report to the Quality Manager.
Essential duties and responsibilities include:
1. Assist the Quality Manager in implementing and maintaining the quality management system.
2. Ensure compliance with requirements in the Quality Manual, Standard Operating Procedures, and other quality documents; provide guidance on quality-related issues.
3. Conduct internal audits, close audit findings promptly, create audit reports, and determine appropriate corrective and preventive actions.
4. Create, maintain, and distribute quality documentation, such as standard operating procedures.
5. Participate in the New Product Introduction team, generating quality documentation.
6. Manage process deviations, non-conformances, supplier complaints, re-works, CAPA, rejects, and change notices.
7. Collaborate with Production to address quality concerns, review non-conforming products, and recommend dispositions.
8. Monitor specific production areas regularly to ensure products are manufactured and sterilized according to quality standards.
9. Liaise with sterilization subcontractors for routine activities and testing.
Qualifications
* Degree in Quality, Science, or Engineering.
* Experience in a Quality role within a manufacturing environment is advantageous.
* Knowledge of ISO 13485, FDA Part 820, and Medical Device Directive (93/42/EEC) is beneficial.
* Experience with EO and gamma sterilization processes, including ISO 11135 and ISO 11137 standards, is a plus.
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