Senior Quality Associate

Job not on LinkedIn

🕒 September 11

🐎 Kentucky, New Hampshire, +11 more states – Remote

🐎 Kentucky – Remote 🗻 New Hampshire – Remote 🏖️ New Jersey – Remote 🌶️ New Mexico – Remote 🗽 New York – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote 🎸 Mississippi – Remote 🔔 Pennsylvania – Remote 🌴 South Carolina – Remote 🗿 South Dakota – Remote 🤠 Texas – Remote ☕ Washington – Remote

💵 $92k - $102k / year

⏰ Full Time

🟠 Senior

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

👻 Ghost score 4%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Aurion Biotech

WebsiteLinkedInAll Job Openings

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

• Support implementation, maintenance, and improvement of the Quality Management System • Support Contract Development and Manufacturing Organization (CDMO) and Contract Testing Lab (CTL) management • Author and review Standard Operating Procedures (SOPs) • Provide Quality Onboarding training • Support vendor management activities • Review and approve vendor documentation • Review executed manufacturing records in support of product disposition • Support computer system validation activities • Support quality performance and continuous improvement activities • Assist in compiling metrics for Quality Management Review • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree in Biology, Chemistry or other relevant scientific discipline preferred • 4+ years of full-time cGMP Quality Assurance experience • Travel required up to 35% • Experience with eQMS (e.g., ACE, TrackWise) • Working knowledge of current industry practices and standards in an FDA-regulated biotechnology company • Excellent record keeping and documentation skills • Strong communication skills, both verbal and written, with the ability to concisely present information in cross-functional settings • Experience working with CDMOs preferred • Proficient use of MS Office products • Ability to rapidly adapt to changing environment and circumstances requiring flexibility, tolerance, and a great sense of urgency while ensuring that all cGMP and regulatory requirements are met • Ability to work effectively both independently and with other team members

🏖️ Benefits

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