Supplier Quality Support Specialist

Job not on LinkedIn

🔥 0 minutes ago

❄️ Minnesota – Remote

❄️ Minnesota – Remote

💵 $38.5k - $52.9k / year

⏱ Part Time

🟢 Junior

🟡 Mid-level

💝 Customer Support

🚫👨‍🎓 No degree required

👻 Ghost score 0%

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Solventum

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

📦 Logistics

💼 Consulting

Healthcare • Logistics • Consulting

Solventum is a healthcare-focused company renowned for its innovative solutions aimed at improving medical and oral care outcomes. The company offers a variety of medical technologies, including advanced wound care, surgical solutions, and sterilization products. Solventum also provides advanced oral care solutions, health information and technology services, and purification and filtration products for biopharmaceutical applications. Furthermore, Solventum places a strong emphasis on sustainability and education, providing resources and training for healthcare professionals globally. Their commitment to innovation and better healthcare has made them a leader in the healthcare industry, dedicated to enhancing patient safety and healthcare efficiencies.

📋 Description

• Establish, update, and manage documentation controls for supplier quality • Maintain, update, and distribute policies, procedures, supplier quality records, and other controlled documents through electronic document management systems • Conduct document audits and monitor records for compliance with internal requirements and external regulations and standards, including ISO, FDA, and OSHA • Help maintain documentation readiness for audits and inspections • Verify documentation completeness and accuracy prior to release • Incorporate approved changes into databases • Generate standard and custom reports • Partner with quality, engineering, manufacturing, and operations teams to resolve documentation discrepancies • Implement procedural changes and maintain training documentation • Support continuous improvement initiatives

🎯 Requirements

• High School Diploma/GED or higher (completed and verified prior to start) • Two (2) years of combined experience in document control, quality systems, coordination support, or records management • Associate's degree or higher in Business, Quality, Engineering, Life Sciences, or a related discipline (additional qualification) • Experience working in a regulated environment, such as medical devices, pharmaceuticals, healthcare, manufacturing, or quality systems • Experience applying document control processes and quality management system requirements • Experience applying ISO standards, FDA regulations, or other regulatory requirements • Experience using electronic document management systems (EDMS), database applications, and document control systems • Experience managing multiple priorities, deadlines, and documentation activities simultaneously • Experience communicating and collaborating with cross-functional stakeholders through verbal discussions, presentations, and written communications • Experience using Microsoft Office applications, including Word, Excel, Outlook, and PowerPoint • Experience maintaining document accuracy, consistency, and compliance within a controlled environment • Experience working independently while supporting cross-functional stakeholders in a fast-paced environment • Must be legally authorized to work in country of employment without sponsorship for employment visa status

🏖️ Benefits

• Medical, Dental & Vision • Health Savings Accounts • Health Care & Dependent Care Flexible Spending Accounts • Disability Benefits • Life Insurance • Voluntary Benefits • Paid Absences • Retirement Benefits • Up to 5% domestic/international travel may be included