Job Details:
Validation Engineer
Validation Engineer to assist in the development of commissioning and qualification protocols for biotech, pharmaceutical manufacturing equipment.
Bachelor’s Degree in Engineering or other.
Several plus years of experience working with biotech, pharmaceutical automation and qualification.
Experience developing Commissioning and Qualification protocol based on design documents.
Understanding of Biotech, Pharmaceutical manufacturing processes and equipment.
Experience with Rockwell Automation Allen-Bradley products required (ControlLogix, Studio 5000, RSLogix 5000, RSLogix 500, PLC5, SLC500, Factory Talk, FTView, MES Solutions, PanelView Plus, etc.)
Understand P&IDs, Process Flow Diagrams and pneumatic drawings. GMP and Validation.
Excellent presentation and communication skills with the ability to converse with a diverse team of persons. Quick learner, the ability to adapt and make changes. A willingness to travel to and from client sites. Self-driven with the ability to work independently.
Key words – Engineer, Validation, Systems Integration, Automation and Controls, Biotech, Pharmaceutical facilities and their equipment – bioreactors, mixing tanks, clean utilities, filtration systems, piping and instrumentation (P&ID) is a plus. Any of these skills are a plus. Rockwell Automation, Controls Engineering, Systems Integration, Allen-Bradley PLC’s, HMI’s. Siemens S7 PLC Systems, FactoryTalkView ME/SE is a plus. US Citizenship, Perm Resident Green Card Holder is required.
If interested please send a copy of your resume as a word doc attachment or PDF to steve@libertyjobs.com. Steve Moore – call or text 484-567-2081. You can also connect with me on LinkedIn https://www.linkedin.com/in/stephenemoore/. I have other positions available across the USA for Automation and Controls Engineers, Rockwell Automation, Allen Bradley, DeltaV Engineers, etc. Validation and Commissioning Engineers, Electrical and Mechanical Engineers, Robotics Engineers, BAS, HVAC, MEP, Construction, etc.