Overview / Responsibilities* Our CQV group at Wood is growing and we are adding to our well respected and established team of Senior CQV / Validation Specialists. We are looking for candidates experienced in CQV / Validation within the pharmaceuticals, biopharmaceuticals, vaccines, and aseptic processing areas. If you are interested in working with a global leader in life sciences and possess the skill and drive to flourish in a dynamic and exciting environment, apply today! *In addition to candidates from the Northeast Region, we also welcome candidates from all regions to apply who are open to 100% travel to be on client sites (per diem included).* Key Responsibilities Preparation and execution of CQV life cycle deliverables, URS / DR / DQ / R
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