Quality Control Analyst (Temporary Position)

Description

Summary: Join as a Quality Control Analyst to ensure product safety and compliance in a dynamic laboratory, supporting pharmaceutical release and stability. Highlights: 1. Safeguard patient health by ensuring highest product safety standards 2. Perform analytical testing of drug products and materials 3. Collaborate with cross-functional teams to maintain quality standards ### **Summary** \#LI\-Onsite Location: Zaragoza – La Almunia, Spain Relocation Support: This role is based in Zaragoza – La Almunia, Spain. Novartis is unable to offer relocation support: please only apply if accessible. Bring quality to life in a role where your expertise safeguards patient health. As a Quality Control Analyst, you will ensure products meet the highest standards of safety and compliance while working in a dynamic laboratory environment. This is a temporary opportunity where your analytical skills will directly support the release and stability of pharmaceutical products, contributing to Novartis’ mission to reimagine medicine, with availability required to support a 24/7 operation. ### **About the Role** **Key Responsibilities** * Perform analytical testing of drug products, finished goods, and materials following approved procedures and standards * Document laboratory activities and results accurately in line with Good Manufacturing Practice requirements * Manage sample storage, tracking, and handling to ensure integrity and compliance * Conduct stability testing and maintain proper documentation of stability studies * Investigate and report technical complaints, adverse events, and quality issues within 24 hours * Ensure full adherence to Standard Operating Procedures and regulatory guidelines at all times * Support audit and inspection readiness through consistent compliance and documentation practices * Monitor deadlines and ensure timely completion of all testing and reporting activities * Identify and implement process improvements to enhance efficiency and reduce operational costs * Collaborate with cross\-functional teams to maintain quality standards and resolve issues effectively **Essential Requirements** * Degree in Chemistry, Pharmacy, or a related scientific field * Experience in quality control within a pharmaceutical or regulated manufacturing environment * Knowledge of Good Manufacturing Practice and quality standards * Hands\-on experience with analytical laboratory techniques and equipment * Ability to follow Standard Operating Procedures with high attention to detail * Strong problem\-solving skills and ability to manage competing priorities * Intermediate level of English, with good reading and writing skills **Desirable Requirements** * Experience with stability testing and lifecycle management of pharmaceutical products * Familiarity with audit and inspection processes within regulated environments **Commitment to Diversity and Inclusion:** Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve **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\) Advanced Accelerator Applications Iberica S.L.U. Functional Area Quality Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No