Validation Engineer
Katalyst CRO · Houston, TX · Today
On-siteEngineeringContract
Roles & Responsibilities
- 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 & Experience
- Bachelor's degree in Engineering (Chemical, Biomedical, Mechanical, or related discipline).
- 26 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.