Quality Control Analyst I

COMPANY OVERVIEW

Vyriad 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:

No

DUTIES AND RESPONSIBILITIES:

• 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.
• Involved in reagent management, routine maintenance of laboratory equipment, and performing robust sample tracking/management.
• Document all testing activities accurately in accordance with cGMP and Good Documentation Practices (GDP).
• Support validation status of release assays, and product stability
• Participate in laboratory housekeeping, calibration, and quality initiatives.
• Work under direct supervision while learning QC systems, methods, and compliance expectations.
• Additional duties as assigned.

EDUCATION AND EXPERIENCE REQUIREMENTS

• Bachelor’s degree in a science related field.
• Minimum of 1 year in an industry or a professional setting incorporating GDP.

REQUIRED SKILLS AND/OR QUALIFICATIONS:

• Familiarity with aseptic technique, basic molecular biology, or analytical methods preferred.
• Familiarity with ALCOA+ Principles of GDP, with familiarity of cGMP preferred
• 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.
• Must have demonstrated capacity to comprehend complex protocols and reports, and programs
• Must be flexible in adapting to a variety of responsibilities, work assignments, and priorities.

PHYSICAL REQUIREMENTS:

• Prolonged periods of standing at laboratory benches.
• Prolonged periods of sitting at a desk and working on a computer.
• Must be able to lift up to 15 pounds at times

WORK SCHEDULE:

• Weekends or weeknight work is occasionally required depending on the production schedule or process needs.

BENEFITS:

• Group Healthcare Plan, including company paid dental and vision.
• Short- and long-term disability, life and AD&G insurance.
• Simple IRA with employer match
• Educational assistance program
• Holiday and PTO

Job Type: Full-time

Pay: $52,000.00 - $67,000.00 per year

Benefits:

• 401(k) matching
• Dental insurance
• Employee assistance program
• Flexible schedule
• Flexible spending account
• Health insurance
• Health savings account
• Life insurance
• Paid time off
• Parental leave
• Retirement plan
• Tuition reimbursement
• Vision insurance

Education:

• Bachelor's (Required)

Experience:

• Good Documentation Practices (GDP): 1 year (Required)
• Quality control: 1 year (Required)

Ability to Relocate:

• Rochester, MN 55901: Relocate before starting work (Required)

Work Location: In person