Associate Validation Engineer
Core
Support planning, coordination, and execution of validation activities for customer, facility, and research projects in a highly regulated sterilization environment.
Role type
Associate Validation Engineer
Builds
Validation protocols, reports, technical documentation, and compliant validation records for medical devices and pharmaceutical products.
Domain
Life Sciences / Medical Devices / Sterilization Services
Required skills
Validation protocol writing and execution, Quality Management Systems knowledge, Data analysis, Equipment qualification (IQ/OQ/PQ), Regulatory compliance (FDA/ISO), Organizational skills
Preferred skills
Sterilization validation experience, FDA and ISO regulatory knowledge, Equipment qualification project support
Technologies
Validation systems, Data analysis tools
Responsibilities
Review validation protocols for feasibility and compliance, Coordinate and execute validation studies, Collect and analyze validation data, Prepare validation work instructions, Support equipment calibration and requalification, Perform hands-on validation activities in operational areas, Maintain validation records, Assist with investigations and corrective actions, Collaborate with internal teams and external customers
Seniority
Junior to Mid-level, hands-on IC