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Vyriad, Inc.

COMPANY OVERVIEWVyriad is an early stage biotechnology company focused on curing cancer using potent, safe and cost-effective cancer therapies utilizing engineered replication competent viruses designed to selectively and rapidly destroy cancer. Revolutionizing cancer treatment is our long-term goal, requiring curiosity, perseverance, an openness to challenging convention and a commitment to excellence. The challenges are complex, the work pace is fast, and progress is seldom a straight line. All of this makes for an exhilarating environment of collaboration, discovery and fun.GENERAL JOB DESCRIPTION:Responsible for performing routine analytical testing of various sample types, including raw materials, intermediates, and drug substance/products to ensure compliance with GMP and regulatory standards. This analyst position is ideal for an individual transitioning into Quality Control with a baseline understanding of biologic therapeutics and cGMP. The QC Analyst I will execute established analytical methods, maintain accurate records, and uphold the highest standards of laboratory safety and data integrity. Experience in cell-based assays and/or PCR-based analyses is preferred.SUPERVISORY RESPONSIBILITIES:NoDUTIES AND RESPONSIBILITIES:<ul><li>Perform and maintain test systems for GMP manufacturing, and performing assays related to in-production and post-production product quality. Assays in the areas of molecular, biochemical, or cell-based systems.</li><li>Involved in reagent management, routine maintenance of laboratory equipment, and performing robust sample tracking/management.</li><li>Document all testing activities accurately in accordance with cGMP and Good Documentation Practices (GDP).</li><li>Support validation status of release assays, and product stability</li><li>Participate in laboratory housekeeping, calibration, and quality initiatives.</li><li>Work under direct supervision while learning QC systems, methods, and compliance expectations.</li><li>Additional duties as assigned.</li></ul>EDUCATION AND EXPERIENCE REQUIREMENTS<ul><li>Bachelor&rsquo;s degree in a science related field.</li><li>Minimum of 1 year in an industry or a professional setting incorporating GDP.</li></ul>REQUIRED SKILLS AND/OR QUALIFICATIONS:<ul><li>Familiarity with aseptic technique, basic molecular biology, or analytical methods preferred.</li><li>Familiarity with ALCOA+ Principles of GDP, with familiarity of cGMP preferred</li><li>Should be detail-oriented and have the ability to work independently and productively under general direction, routinely exercise initiative and sound judgment to contribute to team objectives.</li><li>Must have demonstrated capacity to comprehend complex protocols and reports, and programs</li><li>Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities.</li></ul>PHYSICAL REQUIREMENTS:<ul><li>Prolonged periods of standing at laboratory benches.</li><li>Prolonged periods of sitting at a desk and working on a computer.</li><li>Must be able to lift up to 15 pounds at times</li></ul>WORK SCHEDULE:<ul><li>Weekends or weeknight work is occasionally required depending on the production schedule or process needs.</li></ul>BENEFITS:<ul><li>Group Healthcare Plan, including company paid dental and vision.</li><li>Short- and long-term disability, life and AD&amp;G insurance.</li><li>Simple IRA with employer match</li><li>Educational assistance program</li><li>Holiday and PTO</li></ul>Job Type: Full-timePay: $52,000.00 - $67,000.00 per yearBenefits:<ul><li>401(k) matching</li><li>Dental insurance</li><li>Employee assistance program</li><li>Flexible schedule</li><li>Flexible spending account</li><li>Health insurance</li><li>Health savings account</li><li>Life insurance</li><li>Paid time off</li><li>Parental leave</li><li>Retirement plan</li><li>Tuition reimbursement</li><li>Vision insurance</li></ul>Education:<ul><li>Bachelor's (Required)</li></ul>Experience:<ul><li>Good Documentation Practices (GDP): 1 year (Required)</li><li>Quality control: 1 year (Required)</li></ul>Ability to Relocate:<ul><li>Rochester, MN 55901: Relocate before starting work (Required)</li></ul>Work Location: In person

Quality Control Analyst I

Join Vyriad, Inc. and explore 1   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.

Vyriad, Inc.

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Quality Control Analyst I