Lab System Support Engineer

The CQA Vendor Oversight and Quality Assurance Lead role will own the quality oversight of external partners supporting R&D and regulated activities (e.g., CROs, CMOs, laboratories, technology vendors). Lead the end-to-end vendor lifecycle-due diligence, qualification, quality agreements, risk based monitoring, issue management, and continuous improvement-ensuring adherence to GLP/Google Cloud Platform/GMP/GVP, data integrity and applicable regulations. This role partners closely with Clinical,

Must Have Technical/Functional Skill 810 years of experience in Computer System Validation (CSV) in regulated (GxP) environments (Pharma / Biotech / MedTech). Hands-on experience with validation deliverables: VMP/VP, URS/FS/DS, risk assessments, RTM, IQ/OQ/PQ protocols and reports. Strong knowledge of 21 CFR Part 11 and EU Annex 11; ALCOA+ data integrity principles. Experience validating SDLC/CSV across system types (e.g., LIMS, MES, QMS, ERP, DMS, Lab instruments, cloud/SaaS applications). Fami

Job Summary: Shop Floor CSV/CSA Lead/Engineer responsible for leading and executing validation deliverables across the lifecycle in regulated manufacturing and laboratory GMP/GLP environments. The role includes automation/controls validation, risk-based validation activities, audit readiness, data integrity compliance, and coordination with IT/OT teams for validated systems. Roles & Responsibilities: Lead and execute validation deliverables including risk assessment, validation planning, require

MES Validation Engineer W2 Only role.Candidates must be authorized to work in the United States.Sponsorship is not available for this position.We are seeking an experienced MES Validation Engineer to support the deployment and validation of Manufacturing Execution Systems (MES) within a GMP-regulated pharmaceutical environment. The ideal candidate will have strong experience in CSV, MES validation, PharmaSuite, and validation lifecycle activities. Key Responsibilities Develop, execute, and docum