Industrial Automation Engineer I/II/III/Senior

Our purpose is to bring hope to life by enabling life-changing therapies for patients around the globe creating a healthier and happier tomorrow. Our mission is to work side by side with our customers in order to improve patients lives by bringing new biopharmaceuticals to market.

JOB SUMMARY:

TheAutomation Engineer I II III and Senior is responsible for improving workforce productivity consistency and quality by anticipating and eliminating potential delays through planning scheduling and coordination of processes maintenance calibration resources parts materials and equipment or control system access.

This position is responsible for the installation modification and upgrade of automation systems ensuring that all systems are operating correctly. In addition this position is responsible for developing and designing the concept selecting and programming controllers and ensuring the proper communication between different automation system components simulating installing testing and managing electrical or mechanical automation components and finally monitoring and troubleshooting the automation processes on an ongoing basis.

ESSENTIAL JOB DUTIES & RESPONSIBILITIES

• Lead/participate in the design integration implementation testing commissioning and evaluation of new and existing automation systems.
• Manage automation projects and other resources.
• Simulate and test automated systems equipment or processes.
• Design engineer test and troubleshoot control systems.
• Lead/participate in problem-solving activities; engineer and implement solutions
• Interact with internal staff and shop floor personnel as needed
• Maintain and enhance system documentation.
• Interface with management other engineers and teams.
• Streamline operations for efficiency cost saving safety and reliability.
• Maintain technical project files.
• Assist with the management of budget expenses and P&L responsibilities
• Develop and manage automation capital projects
• Manage special projects and perform other duties as assigned.

FUNCTIONAL KNOWLEDGE

• Adaptable; must be willing to remain flexible to accommodate changing business conditions work requirements and scheduling needs in a rapidly changing environment.
• Demonstrated attention to detail with the ability to focus on the project or task at hand and consistently deliver error-free results
• Excellent organizational skills with the ability to multitask and prioritize.
• Demonstrated proficiency with all Windows-based programs knowledgeable with any CMMS program
• Excellent verbal and written communication skills; ability to communicate with multi-level audiences.
• Demonstrated ability to write investigations and standard operating procedures (SOPs)
• Versatile with various automation systems (Delta V Allen Bradley PLC SCADA BMS etc.) and data historian (OSI PI Proficy).

REQUIRED EXPERIENCE

• Bachelors degree in automation process control or engineering (Computer Electrical or Mechanical) required; EIT or PE highly desirable
• Professional Automation certification preferred
• FDA/GMP knowledge required.
• Experience with designing installing and troubleshooting complex automation systems as well as leading automation projects.
• Experience identifying new opportunities for automation within the manufacturing process.
• Experience simulating and testing these processes or equipment to ensure they function as desired
• Experience writing reports for senior colleagues outlining new concepts testing outcomes and ongoing efficiency
• Experience programming new automated components (Allen-Bradley Siemens Delta V etc.) to the manufacturing process
• Experience developing and maintaining clear and accurate documentation of automation equipment or processes including commissioning and validation (IOQ)
• Experience in training staff training where necessary typically after implementing new processes or equipment or making changes to existing ones
• Experience troubleshooting automated processes or equipment when errors occur
• Experience working on the design of plant systems such as Purified Water HVAC Steam Compressed air and Chilled water systems in addition to equipment such as reactors mixers centrifugal pumps
• Experience using CMMS systems (Maximo BMRAM etc.) and Rockwell Automation software would be a plus.

COMPENSATION RANGE:

• Level I

0-2 Years Experience: $83920 - $115390

• Level II

3-5 Years Experience: $94000 - $129250

• Level III

6-8 Years Experience: $108080 - $148610

• Senior

8 years Experience: $124320 - $170940

Our culture at AGC Biologics is defined by the six core values: Knowledge Trust Quality Ingenuity Accountability and Teamwork. Our core values stem from our team members and are embedded into our DNA. They provide a common language and understanding of how we as an organization are connected across three continents. Our core values serve as a compass and reminder of how we achieve our purpose of bringing hope to life for patients around the globe.

AGC Biologics is a leading global biopharmaceutical Contract Development and Manufacturing Organization (CDMO) with a strong commitment to delivering the highest standard of service as we work side-by-side with our clients and partners every step of the way. We provide world-class development and manufacture of mammalian and microbial-based therapeutic proteins plasmid DNA (pDNA) messenger RNA (mRNA) viral vectors and genetically engineered cells. Our global network spans the U.S. Europe and Asia with cGMP-compliant facilities in Seattle Washington; Boulder and Longmont Colorado; Copenhagen Denmark; Heidelberg Germany; Milan Italy; and Chiba Japan. We currently employ more than 2500 employees worldwide. Our commitment to continuous innovation fosters the technical creativity to solve our clients most complex challenges including specialization in fast-track projects and rare diseases. AGC Biologics is the partner of choice. To learn more visit.Want to keep posted about our growth and learn more about our company Follow us on LinkedIn and give us a quick Like on Facebook!

AGC Biologics offers a highly competitive compensation package and a friendly collaborative culture that values personal initiative and professional achievement. AGC Biologics is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to age ancestry color family or medical care leave gender identity or expression genetic information marital status medical condition national origin physical or mental disability political affiliation protected veteran status race religion sexual orientation or any other characteristic protected by applicable laws regulations and ordinances.