Innovative Consulting Inc. is a global software and engineering consulting firm providing professional services in: Automation, Manufacturing Execution Systems (MES), and Smart Manufacturing. With combined 20+ years of experience in cGMP and FDA regulated industries, our growing and dedicated team of engineers continue to deliver innovative automation related solutions and expertise to plan, design, implement, and maintain projects in alignment with industry standards. We provide professional support and companionship for consulting services, project governance, and accelerating customer solutions in Automation, Manufacturing Systems & Information Technology. We provide client services that include Automation & IT Strategy, Concept Design, Project Execution, Service & Support, Life Cycle Planning & Optimization Services.
Core Responsibilities • Perform automation, instrumentation and control engineering design services for existing facility projects, including upgrades and capacity expansions, equipment upgrading and replacement. • Produce and review design drawings and specification documents (URS, FS, DS, etc.). • Generate, execute, and review design testing, generate and participate in functional specification testing, and perform field inspection services. • Generate, execute, and review Installation, Operational, and Performance Qualification protocols. • Generate, review, and approve GMP Lifecycle Documents (e.g. risk documents, trace matrices, periodic review, etc.) • Execute and track progress of change records. • Manage personal project activities (design and qualification) following client business processes to deliver results that are right first time, on-time with schedule requirements and reconciled to the budget. • Troubleshooting of automation and critical process utility systems. • Lead plant operations to assess discrepant events and changes for automation impact, deliver automation solutions to resolve operational issues, assist in troubleshooting and providing real time on floor support of manufacturing operations, participate in site coordination meetings and attend network meetings.
Required Qualifications • Bachelor's or Master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 5 years' experience, or Master's degree in Engineering (Chemical, Mechanical, Electrical, or Computer Science preferred) and 4 years' experience. • Minimum of 7+ years in Life Sciences, Biotech background preferred, Delta V • Minimum of 5 years in the pharmaceutical/biotech industry & GMP experience. • Minimun of 7+ years of Delta V coding
Additional Details • Employment Type: Full time with ICI