
Senior Validation Engineer
- Thousand Oaks, CA
- $86,500-135,960 per year
- Permanent
- Full-time
- Be a Validation Engineering representative and technical subject matter expert (SME) on cross-functional and multi-site teams related to equipment, systems, utilities, facility, and computerized systems as applicable to its assigned role.
- Create validation documentation including SOPs, risk assessments, traceability matrices, and validation master plans.
- Develop validation protocols (IQ/OQ/PQ) for computer systems as applicable to its assigned role.
- Apply advanced theory, technical principles, and expert judgment to address a broad range of problems.
- Troubleshoot and direct the resolution of Validation issues by fostering effective interdepartmental and cross-functional partnerships.
- Maintain a state of inspection readiness and act as SME in Health Authority inspections.
- Approval of commissioning documents, including but not limited to commissioning protocols and reports.
- Evaluate and leverage testing to qualification activities.
- Generate, execute, and manage the detailed project plans and timelines for the execution of CD/DQ/IQ/OQ/PQ/CV/Validation Maintenance, change management activities and their associated documentation.
- Support departmental and capital project validation activities.
- Provide key performance indicators data in a predetermined frequency.
- Owner of change control task of validation activities.
- Execute validation activities aimed at improving Right First-Time.
- Present and provide rationale for the completed work during periodic audits and Health Authority inspections.
- Coordinate and perform tactical activities, including sample collection, coordinating with cross-functional support teams, retrieving data and results, completing documentation, as required per protocols.
- Coordinate and perform equipment and system re-qualification according to procedures and predetermined timelines.
- Foster an environment that encourages continuous learning. Maintain expertise as necessary to stay abreast of technical and industry advancements.
- Support EHS programs and own CAPA records as needed.
- Accountable for behaviors as described in Takeda Standards, policies, and procedures.
- BS engineering with 8+ years' experience in validation.
- Experience with systems like LIMS, MES, ERP, SCADA, or DCS (e.g., Delta V) for computer systems validation engineers.
- Advanced knowledge of equipment, systems, facilities, and utilities in a regulated environment is required. Advanced knowledge of commissioning and qualification of equipment, systems, computerized systems, facility, and utilities is required.
- Familiarity with software development lifecycle (SDLC) and validation tools.
- Knowledge of GAMP 5, FDA 21 CFR Part 11, and other regulatory frameworks.
- A strong technical and/or engineering knowledge, as well as strong ability to work collaboratively with interfaces to Process Engineering, Quality, Project Managers, Facilities, Automation, and other groups.
- Technical expertise to define validation approaches and execution of system validation activities in accordance with cGMP and applicable regulations, procedures, and industry guidance.
- Advanced understanding of data and statistical analysis of validation test results.
- Basic understanding of data and statistical analysis of validation test results.
- Knowledge of cGMPs or equivalent regulations, validation associated regulations, guidelines, and best practices.
- Proficient in Microsoft Word and Excel, computer software.
- Work in a controlled environment requiring special gowning and wear protective clothing over the head, face, hands, feet and body. This may include additional hearing protection for loud areas.
- Need to remove all make-up, jewelry, contact lenses, nail polish and/or artificial fingernails while in the manufacturing environment.
- Work in a cold, wet environment.
- Work multiple shifts, including weekends, or be asked to work supplemental hours, as necessary.
- Work around chemicals such as alcohol, acids, buffers and Celite that may require respiratory protection.
- The overall physical exertion of this position is light work.
- Able to work in controlled or clean room environments requiring special gowning.
- May be required to work or be assigned to a different shift as needed.
- May require availability outside regular business hours.
- Pace may be fast and job completion demands may be high.