Validation Engineer (Entry-Level)Supports validation activities across Manufacturing, QC (Analytical & Micro), and Facilities in a GMP-regulated biopharma environment. Focuses on developing, executing, and documenting validation for equipment, systems, and processes to ensure compliance with cGMP and regulatory standards.Key Responsibilities:Assist with validation lifecycle activities: IQ/OQ/PQ, process, cleaning, and CSVGenerate and execute validation protocols and reports (including vendor docs)Support equipment onboarding and verificationParticipate in risk assessments (e.g., FMEA)Coordinate with cross-functional teams (Manufacturing, QC, QA, Facilities)Assist with deviations, root cause analysis, and CAPAMaintain compliant documentation and support audit/inspection readinessQualifications:Bachelor's in engineering or life sciences0–2 years GMP experience (internships acceptable)Preferred:Exposure to GMP, FDA regs (21 CFR 11, 210, 211), validation, or cleanroom environmentsFamiliarity with risk tools like FMEAKey Skills:Technical writing, attention to detail, organizationCross-functional communicationProblem-solving and willingness to learnWork Environment:100% onsite (Los Angeles)Mix of office and cleanroom (ISO 7/8) workOccasional off-hours/weekend supportRequires PPE use and facility/equipment access (including rooftops/utilities)