Job Details:
Validation Engineer
Validation Engineer to assist in the development of commissioning and qualification protocols for biotech process manufacturing equipment. Development of Commissioning Plan and Qualification Protocols (IQ, OQ, PQ). Review of technical documentation in order to align with GMP and Commissioning and Qualification requirements. Coordinate activities within project team. Development of reports. Perform risk assessments. Knowledge of GMP. Experience with commissioning, qualification, and validation of systems running on DeltaV and Rockwell Automation platforms. Knowledge of S88 Batch standards. Experience with Biotech process 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.
This position requires an Engineering Degree, Life Sciences, biotech, pharmaceutical, batch process, etc.
Key words – Engineer, Validation, (IQ, OQ, PQ) Systems Integration, Life Sciences, Biotech, Pharmaceutical, Batch Process, bioreactors, mixing tanks, clean utilities, filtration systems, piping and instrumentation (P&ID).
If you have any of these skills it's a plus. DeltaV, Rockwell Automation, Controls Engineering, Systems Integration, Allen-Bradley PLC’s, HMI’s. Siemens S7 PLC Systems, FactoryTalkView ME/SE.
To apply, please send a copy of your 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.