Site Automation Engineer responsible for robotic assembly systems performance. Collaborating with customers and internal teams at Bright Machines.
About the role
- Automation Team Lead managing all on-site industrial controls systems at Zoetis. Focused on compliance and efficiency in automation for pharmaceutical standards.
Responsibilities
- Support and oversee management of all on-site industrial controls systems BMS, PMS, EMS and PCS infrastructure and RLAN IT/OT architecture
- Lead and maintain Automation master plan for the entire site
- Manage life cycle and change control process for all automation control systems
- Provide support to maintenance teams for troubleshooting instruments and control systems
- Develop training programs for instrumentation and control systems to enhance team skills
- Manage vendors and consultants, ensuring contracts contain technical specifications
- Stay updated on developments in instrumentation and control technology
- Interface with users, peers, and management for appropriate input and integration of standards
- Provide technical expertise during regulatory audits
- Author, review, revise, or approve Standard Operating Procedures (SOPs)
- Oversee implementation of essential automation infrastructure from conception to completion
- Lead/Coordinate Factory Acceptance Test and Site Acceptance Test for all automation
Requirements
- Bachelor’s degree in electrical engineering, chemical engineering, automation engineering, or a related field is required
- 10 years managing automation systems experience in automation engineering, particularly in the pharmaceutical or biotechnology sectors is required
- Demonstrated experience in the design, implementation, and maintenance of automation systems within a GMP (Good Manufacturing Practice) environment
- Proficiency in PLC (Programmable Logic Controller) programming, SCADA (Supervisory Control and Data Acquisition) systems, DCS (Distributed Control System), and other automation technologies
- Knowledge of industry standards such as ISA-88, ISA-95, and GAMP (Good Automated Manufacturing Practice)
- Familiarity with regulatory requirements, including FDA regulations, cGMP (current Good Manufacturing Practice), and other relevant guidelines governing the pharmaceutical industry
- Technical Experience leading and managing automation projects from concept through commissioning, ensuring adherence to project timelines and budgets
- Understanding of equipment and system validation processes, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification)
- Ability to troubleshoot complex automation issues, identify root causes, and implement effective solutions
- Basic understanding of IT/OT (Information Technology/Operational Technology) digital concepts, with the ability to integrate automation systems EMS, DCS, PCS and BMS into broader digital frameworks
- Efficient Project Management skills
- Excellent written and oral communication skills for concise and practical presentations
- Proficiency in English, both written and oral.
- Computer proficiency with email; internet/online training; working knowledge of Microsoft Office, including Word and Excel; familiarity with manufacturing software programs
Benefits
- Competitive healthcare and retirement savings benefits
- An array of benefits, policies and programs to support employee well-being in every sense, from health and financial wellness to family and lifestyle resources
Job title
Job type
Experience level
Salary
Not specified
Degree requirement
Location requirements
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