Engineer, Quality Engineering

Join our team to support impactful projects that drive continued process verification and monitoring at our GMP facility. This role involves cross-functional collaboration and the implementation of data-driven solutions in a commercial manufacturing environment.

• Manufacturing process experience in cell therapy or biologics (GxP)
• Data Analysis / Process Monitoring (JMP, Python or similar statistical tools)
• Computer System Validation within the biotechnology or pharmaceutical industry
• Experience in implementing data solutions in commercial manufacturing environments
• Clear communication across all levels
• Prior work experience at client or in client's Industry

Applicants must be able to work directly for Artech on W2

• cGMP experience
• Lean/Six Sigma certification
• Education in Immunology

• Provide support for data extraction and verification to enable automated tools for CPV and process monitoring
• Collaborate with site MSAT, IT, vendors, and global teams to ensure successful implementation of projects
• Gather functional requirements and architect end-to-end solutions for scaling analytical capabilities
• Support routine process monitoring to identify process improvements and efficiency opportunities
• Lead cross-functional and cross-site projects

• Comprehensive health, dental, and vision insurance
• Opportunities for professional development and career growth
• Inclusive and collaborative work environment

For immediate consideration please click APPLY to begin the screening process with Alex.