Quality System and Document Control Specialist

Location: Rochester, Minnesota

Be the bridge between precision and innovation in a fast-evolving biotech company revolutionizing viral, genetic, and cell-based therapies. In this role, you’ll keep the quality heartbeat strong across departments while helping to ensure life-changing therapies reach those who need them most.

Why You Should Apply

• Work at the forefront of viro-immunotherapy research
• Join a tight-knit, fast-moving biotech team making global impact
• Full benefits package including health, dental, vision, and life insurance
• Company-paid short- and long-term disability, AD&D, and Simple IRA with match
• Paid holidays and generous PTO
  
  

What You’ll Be Doing

• Maintain and manage quality documentation in a controlled system
• Monitor and improve Quality Management System (QMS) compliance
• Coordinate quality audits, both internal and external
• Lead training program and documentation review cycles
• Facilitate change control processes and cross-departmental coordination
  
  

About You

• Have GxP and/or CLIA lab experience
• Experience with ISO 9001 and eQMS systems (Qualio is a plus!)
• Comfortable communicating with regulators and scientific staff alike
• Love organizing chaos into crystal-clear compliance
  
  

How To Apply

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to ava@scientificsearch.com and tell me why you’re interested. Or, feel free to email your resume. Please include Job #19279