Quality Manager

Location: Grand Island, Nebraska

Lead quality excellence in a cutting-edge sterile manufacturing environment. My client is seeking a Quality Manager to champion GMP compliance, strengthen quality systems, and guide teams producing life‑sustaining products for the animal health industry. This role sits at the center of manufacturing, validation, and regulatory operations—ensuring every process meets the highest standards of safety and reliability.

• Salary range $100k – $115,000
• Lead quality strategy in a state‑of‑the‑art sterile manufacturing facility
• Strong benefits including health insurance, disability coverage, and retirement plan
• 401(k) with company match and fully vested contributions
• Paid vacation, sick time, seven paid holidays including birthday pay
• Work in a clean, temperature‑controlled environment with a collaborative culture

• Lead and mentor the Quality Systems team while overseeing daily quality operations
• Maintain GMP compliance through SOP creation, revision, and implementation
• Oversee investigations including deviations, OOS events, and CAPA activities
• Manage validation activities including aseptic, cleaning, steam, and analytical validation
• Support internal audits, vendor audits, and regulatory readiness
• Oversee document control, change control, calibration programs, and recall processes

• Bachelor’s degree in applied science, engineering, or related field
• Strong knowledge of FDA regulations and GMP manufacturing
• Experience managing quality management systems and compliance programs
• Familiarity with pharmaceutical or sterile manufacturing processes
• Proficiency with Microsoft Office and technical documentation

We’d love to see your resume, but we don’t need it to have a conversation. Send us an email to  and tell me why you’re interested. Or, feel free to email your resume. Please include Job#19764