Quality Coordinator

Job not on LinkedIn

🕒 6 days ago

🐎 Kentucky, New Hampshire, +10 more states – Remote

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💵 $72k - $79k / year

⏰ Full Time

🟢 Junior

🟡 Mid-level

🦅 H1B Visa Sponsor

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👻 Ghost score 0%

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Logo of Aurion Biotech

Aurion Biotech

51 - 200 employees

Founded 2022

🏥 Healthcare

🏭 Manufacturing

🧬 Biotechnology

💰 $120M Venture Round - Aurion Biotechnologies on 2022-04

Healthcare • Manufacturing • Biotechnology

Aurion Biotech is a clinical-stage company developing first-in-class regenerative cell therapies to restore vision by treating corneal endothelial disease and other causes of blindness. The company focuses on manufacturing-scale cell therapy platforms, using human donor corneal endothelial cells combined with supportive compounds (e. g. , rho-kinase inhibitor) to repopulate the corneal endothelium, reduce reliance on donor tissue, and enable less-invasive alternatives to graft-based keratoplasty. Aurion conducts global clinical trials, holds FDA Breakthrough Therapy and RMAT designations for its lead product AURN001, and aims to expand access to advanced ophthalmic care worldwide.

📋 Description

• Manage and maintain Quality project trackers and milestone reports • Generate status updates and reports for Quality leadership • Request Statements of Work and track approval status • Track Purchase Order approvals and coordinate with Finance, Procurement, and vendors • Monitor PO status and maintain expenditure and contract documentation records • Support vendor onboarding and documentation requirements • Route quality-related documents through review and approval workflows • Ensure documentation is completed, approved, and archived according to procedures and quality standards • Maintain organized electronic records and tracking systems • Coordinate and submit sample shipment requests to testing facilities • Track sample shipments and confirm receipt • Collaborate with Quality Control, Quality Assurance, Supply Chain, Procurement, Finance, and external partners • Perform additional coordination and administrative duties as assigned

🎯 Requirements

• Bachelor's degree with 0–2 years of relevant experience required • Degree in a scientific discipline such as Biology, Chemistry, Microbiology, Biochemistry, Pharmaceutical Sciences, or related field required • Experience in a regulated pharmaceutical, biotechnology, or medical-device environment preferred • Life-sciences Quality Assurance or Quality Control experience highly preferred but not required • Working experience with Smartsheets required • Experience in project coordination, operations support, quality systems administration, or related duties highly preferred • Strong organizational skills and ability to manage multiple priorities • Experience tracking projects, schedules, milestones, and deliverables • Proficiency with Microsoft Office, particularly Excel, Word, Outlook, and PowerPoint • Excellent written and verbal communication skills • Detail-oriented with strong accuracy and follow-through • Ability to work effectively in a fast-paced, cross-functional environment

🏖️ Benefits

• Full health insurance for employees and their families • 401(k) matching • EAP • FSA • Generous PTO • Competitive compensation packages • Paid parking • Subsidized commuter passes • In-office catered lunches • Team events • Community projects

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