Our client in the pharmaceutical industry is seeking a Validation Engineer to join their growing team within the Clinical Supply Chain organization. This person will be responsible for validating sterile manufacturing equipment and critical utilities systems in the pilot plant in King of Prussia, PA. Primary responsibilities include validation lifecycle documentation for GMP manufacturing equipment such as fermenters, bioreactors, and chromatography skids; change management & control in a GMP environment; and requalification of systems such as autoclaves on an annual basis.
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-5+ years of experience as a Validation Engineer within a biopharmaceutical manufacturing environment
-Sterile manufacturing experience (fermenters, bioreactors, chromatography skids)
-Autoclave experience
-Depurination experience
-Bachelor's Degree in Mechanical Engineering, Chemical Engineering, Biology, or related
Benefit packages for this role will start on the 1st day of employment and include medical, dental, and vision insurance, as well as HSA, FSA, and DCFSA account options, and 401k retirement account access with employer matching. Employees in this role are also entitled to paid sick leave and/or other paid time off as provided by applicable law.