Microbiologic Technician

Description

Summary: This role supports all GxP activities within the Quality department by administering quality systems and processes—including documentation, metrics, and action monitoring—and ensuring compliance with Novartis standards. Highlights: 1. Supports all GxP activities within the Quality department 2. Administers quality systems/processes, including documentation 3. Ensures adequate education and GxP knowledge ### **Summary** \~Supports all GxP activities within the Quality department. Administers quality systems/processes, including documentation, metrics, and action monitoring. \~Supports the development of high-quality operational processes. Performs routine GxP/operational compliance activities in accordance with Novartis quality standards. Supports quality projects and initiatives. ### **About the Role** Major Accountabilities \~ Supports applicable Standard Operating Procedures (SOPs), GxP documentation, and records within the Novartis Quality Management System. \~ Ensures integrity of all quality system records and data, as applicable, and fosters collaboration between own team and other functions/departments. \~ Ensures adequate education and GxP knowledge. \~ Updates and maintains relevant information in electronic systems (e.g., change control, documentation, training). \~ Monitors and tracks compliance activities, e.g., CAPAs, actions, metrics, quality plan. \~ Supports quality audits and health authority inspections. \~ Reports technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt. \~ Distribution of marketing samples (if applicable) Key Performance Indicators \~Supports all GxP activities within the Quality department. Administers quality systems/processes, including documentation, metrics, and action monitoring. \~Supports the development of high-quality operational processes. Performs routine GxP/operational compliance activities in accordance with Novartis quality standards. Supports quality projects and initiatives. Work Experience \~QC/QA in pharmaceutical/biotech industry with environmental monitoring and cleanroom areas \~Broad functional scope \~Cross-organizational collaboration Skills \~Technology scouting \~QA (Quality Assurance) \~GMP procedures \~Quality standards \~Quality Control (QC) testing \~Working with ambiguity \~Self-awareness \~Continuous learning \~Technology expertise Language English **Why Novartis:** Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture **Benefits and Rewards:** Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Operations Business Unit Quality Location Spain Site Zaragoza Company / Legal Entity ES45 (FCRS \= ES045\) AAA Ibérica S.L.U. Functional Area Quality Job Type Full time Employment Type Regular Shift Work No VIDEO