Computer System Validation Engineer
- Pharma (Onsite
- Bothell, WA) (Bothell, WA, 98021) | 06/17/26
Easy Apply
Share Job Job Description Computer System Validation Engineer
- Pharma (onsite
- Bothell, WA) We are seeking a Computer System Validation Engineer
- Pharma for a global pharmaceutical client.
You will work cross-functionally to lead and execute validation activities for GxP electronic systems and applications. This role is an individual contributor who will partner with Business Owners, Technical Owners, and Quality to create and manage validation deliverables for electronic systems and applications throughout the validation lifecycle. The CSV Contractor has primary responsibility to ensure that the tasks supporting validation of Manufacturing Execution Systems (MES) are documented in accordance with the relevant procedures and regulations. This is a 40-hour per-week, 12-month contract (extensions possible), 100% onsite role in Bothell, WA and required to be onsite throughout UAT execution. This is a W2 role as a Stage 4 Solutions employee. Health benefits and a 401K are offered.
Responsibilities:
Author, review and/or approve applicable CSV documentation
Assist Business Owners and Technical Owners during test execution, document test failures and ensure testing aligns with internal procedures
Assist Business Owners and Technical Owners to develop requirements and specifications for computerized systems used in GxP operations
Requirements:
4+ years of direct experience with CSV activities, strong knowledge of GAMP / risk-based approaches to validation and good understanding of electronic records and signatures
Strong knowledge on Manufacturing Execution System (MES) validation. Familiarity with MES systems (i.e. Emerson Syncade), ERP systems (i.e. SAP or Oracle) and EBRs (i.e. InfoBatch).
Strong knowledge on development of CSV documentation (Validation Plans, Requirements, Specifications, Assessments, Test Scripts [IQ / OQ / PQ or equivalent], Summary Reports, Trace Matrices, SOPs, etc.)
Knowledge of c
GMP, GXP, GAMP, SDLC
regulations, including 21CFR part 11, and good documentation practices.
Knowledge of pharmaceutical, manufacturing and laboratory systems and equipment that support Biologics and clinical manufacturing.
Knowledge of IT service management platforms to support incident, problem and change IT operational events (i.e. ServiceNow)
Knowledge and exposure to Business Quality Management Systems (i.e. Veeva).
Bachelor's degree in a life sciences or engineering / IT discipline or equivalent industry experience.
