GlaxoSmithKline LLC seeks Validation Supervisor in King of Prussia, PA responsible for the self-directed supervision of the day-to-day operations of Validation team members to support the value stream. Req: Bachelor’s (or for. equiv.) in Biochemical Engineering, Biology or related field + 5 yrs of progressive validation experience along with the following: • 3 yrs exp. in people or matrix leadership consisting of peers, subordinates, or senior personnel in multidisciplinary teams involving scientific, engineering, & operational disciplines; • 3 yrs exp. utilizing current GMP’s, NIH Guidelines & FDA or European validation practices for biopharmaceutical processes & supporting regulatory audits as SME; • 2 yrs exp. in the validation of large-scale bulk biopharmaceutical facilities including cell culture, or microbial fermentation, or protein recovery & purification operations including hands-on experience with single-use systems used in biopharmaceutical processes; and 2 yrs exp. in utilizing industry & validation practices related to technology transfer & product lifecycle including executing technology transfer plans. Resumes to faith.m.donaher@gsk.com; job code: JH.