Job Details:
Validation Engineer
Validation Engineer to assist in the development of commissioning and qualification protocols for biotech, pharmaceutical manufacturing equipment. Experience developing Commissioning and Qualification protocol based on design documents. Understanding of Biotech, Pharmaceutical manufacturing processes and equipment. Experience with Automation Infrastructure and Data Integrity. cGMP, GMP and Validation experience. Knowledge of lab equipment, upstream and downstream bio process equipment, life cycle documents as defined in GAMP 5.
Engineering Degree, 5 plus years’ of experience working in the Life Sciences industries - biotech, pharmaceutical automation and qualification. Excellent presentation and communication skills.
Key words – Engineer, Validation, Systems Integration, Life Sciences - 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.
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 – Engineers, Automation and Controls Engineers, DeltaV Engineers, Validation Engineers, Systems Integration, Electrical and Mechanical Engineers, Robotics Engineer, etc.