
10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 B2B
Biotechnology • Science • B2B
Danaher Corporation is a leading global life sciences and diagnostics innovator that develops and supplies instruments, technologies, software, and services to accelerate scientific research, biotechnology development, and clinical diagnostics. The company operates through businesses focused on biotechnology tools, diagnostics platforms, and life sciences products, leveraging the Danaher Business System and an acquisition-driven strategy to scale technologies and support customers across academia, pharmaceutical and biotech companies, and clinical laboratories.
🔥 0 minutes ago
🌾 Iowa, North Dakota – Remote
💵 $95k - $135k / year
⏰ Full Time
🟠 Senior
🔴 Lead
👔 Manager
🦅 H1B Visa Sponsor
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10,000+ employees
🧬 Biotechnology
🔬 Science
🤝 B2B
Biotechnology • Science • B2B
Danaher Corporation is a leading global life sciences and diagnostics innovator that develops and supplies instruments, technologies, software, and services to accelerate scientific research, biotechnology development, and clinical diagnostics. The company operates through businesses focused on biotechnology tools, diagnostics platforms, and life sciences products, leveraging the Danaher Business System and an acquisition-driven strategy to scale technologies and support customers across academia, pharmaceutical and biotech companies, and clinical laboratories.
• Own the end‑to‑end management of GxP‑regulated manufacturing systems • Ensure manufacturing systems operate in compliance with GxP regulations • Coordinate with the Validation team and govern change management for GxP systems • Partner closely with Quality, Manufacturing, and IT stakeholders to translate operational needs into compliant system capabilities • Oversee operational stability and performance of GxP systems • Manage vendors and service partners supporting GxP systems • Maintain inspection-ready documentation, support internal and external audits and regulatory inspections
• Bachelor’s degree in Information Technology, Engineering, Life Sciences, or a related discipline • At least 8–10 years of experience supporting or managing manufacturing IT systems in regulated environments • Demonstrated experience managing GxP‑regulated systems, including validation support, compliance oversight, and change control in collaboration with Quality and Validation teams • Strong understanding of manufacturing systems (e.g., MES, LIMS, QMS, instruments related, or related manufacturing platforms) • Experience operating within IT service management and quality governance processes • Hands-on software development experience supporting system integrations, automation, or platform enhancements, using technologies such as C#, JavaScript/TypeScript, modern web frameworks (e.g. React), and API‑based integrations.
• paid time off • medical/dental/vision insurance • 401(k) to eligible employees • remote work arrangement
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