Automation Specialist III

Job Description Salary:Overview:The Automation Specialist III is directly responsible for the execution of all automation assignments to fulfill our clients operational and compliance needs. This role requires deep expertise in, with a focus on biotechnology processes, particularly in purification and utilities systems. The ideal candidate will apply advanced engineering principles to the design, implementation, and optimization of automation solutions for manufacturing environments regulated under cGMP standards.Key Responsibilities:Lead the execution of multiple, large-scale automation projects across various client sites.Coordinate and oversee the development, troubleshooting, and continuous improvement of automation systems in biotechnology purification and utility processes.Apply advanced knowledge of systems to optimize bioprocess control and performance.Provide day-to-day management and support of automation systems, including software/hardware integration.Troubleshoot and maintain manufacturing and utility equipment automation systems to ensure reliable operation.Design, develop, and optimize control logic for HMI, SCADA, and PLC systems.Perform inspections, testing, and commissioning of automated systems following SOPs and protocols.Prepare technical documentation, engineering analysis, and project status reports.Collaborate across departments to align automation strategies with overall process goals and regulatory requirements.Provide support for validation and qualification activities for automation systems in accordance with FDA and industry guidelines.Keep current with industry trends and incorporate best practices into automation strategies.Qualifications:BS/BA degree in Engineering, Biotechnology, or a related technical field.Minimum of 6 years of experience in automation roles, with at least 3 years specifically working with DeltaV systems.Proven knowledge of biotech purification processes and utilities systems (e.g., clean steam, WFI, HVAC).Strong background in PLC, SCADA, and standalone systems in GMP-regulated environments.Basic project management knowledge: scheduling, timeline tracking, and milestone delivery.Experience with Microsoft-based systems, SQL, Visual Studio, and AutoCAD is preferred.Excellent interpersonal and communication skills for cross-functional collaboration.Self-motivated, organized, and capable of handling multiple tasks in a dynamic environment.Bilingual: English and Spanish (written and verbal proficiency required).Physical/Mental Requirements:Ability to stand for extended periods during test runs.Capable of working extended shifts, as required.Ability to climb ladders and lift up to 25 lbs.Must wear required gowning and PPE in manufacturing and cleanroom areas to meet GMP and OSHA standards.Equal Employment Opportunity (EEO) Statement:We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.