Validation Engineer IIWe are looking for a Validation Engineer II with experience in the pharmaceutical or biopharmaceutical industry to join our growing team. Roles and responsibilities include:Develop and execute IQ, OQ, PQ validation protocols and reports for equipment, utilities, and facilities.Perform CQV activities, including Temperature Mapping for Controlled Temperature Units (CTUs).Collaborate with Manufacturing, QA, Engineering, and R&D teams.Analyze validation data, investigate deviations, and support CAPA implementation.Prepare validation reports and support internal/external audits.Review and support change controls for validated systems.Education and experience required:Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or related discipline).2–6 years of validation experience in the pharmaceutical or biopharmaceutical industry.Strong knowledge of cGMP, FDA regulations (21 CFR Parts 210, 211 & 820), and ICH guidelines.Hands-on experience with IQ/OQ/PQ and Temperature Mapping of Controlled Temperature Units is required.
Validation Engineer in houston at Unknown Company
This position is listed as full time and onsite.