Avery Dennison Corporation (NYSE: AVY) is a global materials science and digital identification solutions company. We are making possible products and solutions that help advance the industries we serve, providing branding and information solutions that optimize labor and supply chain efficiency, reduce waste, and promote sustainability, circularity, and transparency. We design and develop labeling and functional materials, radio-frequency identification (RFID) inlays and tags, software applications that connect the physical and digital, and offerings that enhance branded packaging and carry or display information to improve the 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 in 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 let us know if we can support you with reasonable accommodations throughout the application process by contacting our team via [emailprotected].
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:
* Assist the Quality Manager in implementing and maintaining the quality management system.
* Ensure adherence to requirements in the Quality Manual, Standard Operating Procedures, and other quality documents, providing guidance on quality-related aspects.
* Conduct internal audits, close out audit findings promptly, create audit reports, and determine corrective and preventive actions.
* Create, maintain, and issue quality documentation, such as standard operating procedures.
* Participate in the New Product Introduction team, generating quality documentation.
* Manage process deviations, non-conformances, supplier complaints, re-works, CAPA, rejects, and change notices.
* Collaborate with Production to resolve quality concerns, review non-conforming products, and recommend dispositions.
* Monitor production areas regularly to ensure products are manufactured and sterilized according to quality documentation.
* Liaise with sterilization subcontractors for routine sterilization and testing activities.
Qualifications
* Degree in Quality, Science, or Engineering.
* Experience in a Quality role within a manufacturing organization is advantageous.
* Knowledge of ISO 13485, FDA Part 820 regulations, and the Medical Device Directive (93/42/EEC) is beneficial.
* Experience with EO and gamma sterilization processes and standards (ISO 11135 & ISO 11137) is advantageous.
We value diversity and inclusion, believing that every voice enriches our workplace. Across our global team, each individual’s unique personality and talents contribute to our collective success. We are committed to equal opportunities and fostering an inclusive environment.
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