Automation Engineer

Biotechnology Centennial, Colorado


About Azzur

Our employees are fueled by an entrepreneurial spirit and the desire to make a difference in the lives of our customers, coworkers and our partners. If you’re ready to put in the work, take personal responsibility and test the limits of what’s possible, we’re ready to provide the reward.

Do What You Love

At Azzur, we look for talented individuals who take pride in the work they do. We foster employee growth by encouraging our employees to focus on doing what they love and what they do best.

Azzur is a GxP compliance and consulting organization dedicated to providing high quality, expertly backed, assistance that drives life science companies to success. We are seeking highly motivated and talented individuals to join our incredible team of skilled problem solvers. Qualified candidates must have a desire to learn, apply, engage, and adapt in the ever-changing healthcare field while simultaneously and organically exuding Azzur’s core values:

Put Others First, Courage to Take Action, Take Personal Responsibility and Have Fun!

This role will be responsible for administration of Environmental Monitoring system, OSIsoft PI Data
Historian, Automation Versioning application platform. The administration activities include data logger integration, integrating standalone automation systems to OSIsoft PI system as well as responsible for version control for PLC programming and critical parameter management.
  • Deliver automation and controls support for daily operations and troubleshooting PD and GMP Manufacturing equipment and other facility related stand-alone equipment
  • Install, configure, and modify data logger integration into our Environmental Monitoring System as well as troubleshoot any events impacting the system
  • Integrate standalone equipment to OSIsoft PI system via various interfaces
  • Manage version control for PLC programming and critical VFD parameter management as well as the qualified Facility Alarm response system
  • Candidates must understand P&IDs, wiring diagrams and I/O configuration, system networking and field devices
  • Manage creation and revision of Protocols, Reports, and Engineering Documents including, but not limited to drawings, user requirement specifications and SOP’s
  • Effectively work with cross departmental stakeholders to achieve departmental goals and objectives
  • Develop and execute validation protocols as well as write technical reports and/or presentations relevant to processing activities and present to various levels of management and regulatory authorities
  • Lead Automaton Projects including the definition of the scope of work and specification development.

  • B.A, B.S. in Engineering or related discipline with at least 5 years of relevant experience or M.S. with at least 2 Years of relevant experience
  • Experience with Data Integration: RESTapi, OSIsoft PI, SQL, OPC and database architecture
  • Experience working with Rockwell/Allen Bradley and Siemens PLC and HMI products
  • Knowledge of facility related engineering disciplines (MEP) in GMP manufacturing environment
  • Excellent verbal and written communication skills applied on a global or multi-national basis
  • Strong interpersonal skills, including the demonstrated ability to manage through influence.