Veristainc is seeking a CQV Engineer to support solution preparation systems in biopharmaceutical manufacturing. The ideal candidate will have over 10 years of experience and strong skills in CQV lifecycle documentation, as well as a bachelor's degree in a related field.
This role also requires collaboration across engineering and quality teams and experience with digital validation platforms like Kneat. Competitive salary and benefits are included.
#J-18808-Ljbffr