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CSV Validation Lead at Zifo. . Define validation Strategy for computerized systems and/or analytical instruments utilized in GxP Space . . Create Validation deliverables such as Validation Plan, Test Protocols, Traceability matrix and execution of protocols.. . Conduct user review meetings. Lead discussions with Quality Assurance and Compliance groups . . Conduct Risk Assessments. Develop and maintain policies and procedures . . Effectively communicate the validation activities and deliverables to the project team, customer stake holders and global team within Zifo . . Act as a liaison between Zifo remote teams and customers in US & Canada . . Participate in internal initiatives around Computer Systems Validation . . . Bachelor or Master’s degree in Life Sciences or Computer Sciences . . 10+ years’ experience with Computer Systems Validation within the pharmaceutical industry is required for this role . . Strong knowledge of GxP Requirements, GLP and GMP regulations, 21 CFR part 11 requirements . . Experience with laboratory or GxP systems validation like ELN, LIMS, QMS etc. . . Company Location: United States.