Automation and Controls Engineer

4 weeks ago

Devens, United States System One Holdings, LLC Full time

Job Title: Automation and Controls Engineer Location: Devens, MA Durantion: Contract to HireMust Haves: Bachelor of Science Degree in chemical or electrical engineering (or related field) is required with a minimum of 5 year of experience, or a minimum of 10 years of practical experience. Experience in the fields of process control and automation with project management experience in the pharmaceutical industry is preferred. Experience with and a thorough understanding of technical concepts, practices and procedures in bulk pharmaceutical manufacturing, and related support systems is strongly preferred.Experience working with Microsoft Office (Outlook, Word, Excel, Project,and Visio) is essential.Must be able to read and understand repair manuals, specifications, drawings, and schematic diagrams and execute timely and accurately.Excellent verbal and written (including technical writing) communication and interpersonal skills are a must.Must have excellent organizational skills and be attentive to detail. Experience in operation, maintenance, troubleshooting and programming of Delta V Distributed Control Systems as well as Allen Bradley and Siemens PLC systems is strongly preferred. Responsibilities: Oversee all phases of automation and control related project design activities. Develop controls portions of User Requirement Documents for all projects.Analyze safety instrumented systems and design safety rated interlock systems. Prepare comprehensive requests for proposals for all controls project work. Manage outside contractors who are employed to complete projects within agreed-upon timelines and budget. Responsible for managing all plant floor level control systems and organizing all architectures, programming, and control systems for future projects.Serve as the facility expert on all plant control systems to enable effective in-house troubleshooting and updates without requiring outside resources. Participate in continual process improvement programs, including minimizing utilities usage. Maintains and updates all automation and control system documentation, including both hardware and software. Maintain a database of current and archive automation programs.Develop standards for automation and communication. Develop master plans for automation on site. Develop and maintain software backup systems and recovery systems. Applies cGMP concepts in association with department specific responsibilities. Ensures all documentation produced are compliant with cGMP standards. Responsible for contributing to audit readiness and for participating in quality audits with FDA, other Regulatory Agencies, and customers, as needed.

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