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Quality Assurance and Compliance Manager
AttindasGreenville, United Statesfull_timeVerifiedPosted 23 Feb 2026
About the role
Attindas Hygiene Partners designs, manufactures, and markets absorbent hygiene products. The company sells adult incontinence and infant diapers, among other products, into the healthcare, retail, and direct-to-consumer channels under brands including Attends, Indas, and Comfees as well as a wide range of private label brands for retailers. Mission: We champion health, dignity and comfort. Vision: To be a global leader in absorbent hygiene by meeting consumers’ diverse needs through effective, affordable and widely available personal care solutions. Our Values: Personal, Agile, Innovative, and Integrity Job Summary: Compliance/Governance/Regulatory:
- Manage company registration, reporting, and documentation for EPR regulations across multiple U.S. jurisdictions.
- Lead development of EPR reporting processes for packaging usage and other regulated materials.
- Lead internal data collection across business units (e.g., Commercial, Operations, Sustainability, Finance).
- Drive action in cross-functional initiatives and the assessment of raw materials process to manage risks.
- Develop tracking systems for compliance reporting and deadlines.
- Stay current through training and global monitoring, including webinars and collaboration with international sites.
- Interpret customer specifications and quality expectations, clearly communicating product and process requirements to manufacturing and cross-functional teams.
- Monitor and manage customer portals, surveys, and questionnaires to ensure alignment with quality expectations.
- Lead collaboration between work groups—such as production, engineering, procurement, supply chain, and quality—to address quality concerns and drive continuous improvement initiatives.
- Actively support customer-facing activities, including site audits, product category meetings, and Unitas projects.
- Manage and maintain QMS documentation, serve as administrator for the corporate electronic QMS, and train business units.
- Guide regulatory compliance, identifying certification requirements and gaps, and acting as a subject matter expert on industry standards.
- Other duties as assigned
- Bachelor’s degree and/or relevant experience
- 3 to 5 years of experience in a quality or regulatory role
- Experience with Quality Management Systems (QMS) such as ISO 9001 or ISO 13485
- Experience analyzing and reporting data
- Knowledge of root cause analysis, corrective/preventive actions (CAPA), and problem‑solving tools.
- Strong attention to detail and analytical thinking
- Effective communication skills for cross-functional collaboration
- Lean Six Sigma Yellow or Green Belt
- Internal auditor certification for ISO standards
- Experience with QMS software
- Previous experience with medical device manufacturing
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