Packaging Specialist

Description

Job Summary: This temporary specialist will coordinate the labeling and packaging of products, ensuring compliance with Good Manufacturing Practices and internal procedures to deliver high-quality medicines to patients. Key Highlights: 1. Coordination of labeling and packaging of finished products 2. Compliance with quality standards and GMP/BPM 3. Pharmaceutical production environment and contamination control ### **Summary** \#LI\-Onsite \- La Almunia \#Temporary Position Help deliver high-quality medicines to patients. As a Temporary Packaging Specialist, you will coordinate the labeling and packaging of products, ensuring compliance with Good Manufacturing Practices and internal procedures. ### **About the Role** **Key Responsibilities:** * Coordinate the labeling and packaging of finished products. * Perform labeling and packaging activities for products. * Responsible for controlling Raw Materials (RM) used in sterile batch manufacturing, e.g., labels, shelf life, and Batch Record (BR) compliance. * Execute production activities in Class D and unclassified areas, following Batch Record instructions, aseptic behavior guidelines, and SOPs/POEs. * Prepare and set up equipment for labeling and packaging activities, as well as for production activities performed in Class D and unclassified areas. * Adhere to behavioral standards and material flow requirements in controlled-contamination areas, especially in the sterile suite, per internal procedures. * Perform cleaning and washing of Class C areas according to established procedures outlined in specific SOPs. * Timely record all activities conducted during the manufacturing process, in accordance with Data Integrity principles and SOP/POE instructions. * Immediately address any unexpected situations, e.g., air pressure drop, temperature or humidity fluctuations, machine stoppage, or deviations from validated standard operations. **Key Performance Indicators:** * Production output aligned with production planning and quality requirements, including GMP/BPM compliance. * Deviations occurring during production. * Absence of critical observations during regulatory authority audits. * Absence of errors when completing required documentation, such as the Batch Record. * Attendance at technical and GMP/BPM training sessions. **Essential Requirements:** * Prior experience in pharmaceutical production or manufacturing environments * Knowledge of Good Manufacturing Practices and quality standards * Ability to accurately follow detailed procedures and production documentation * High attention to detail and commitment to quality and safety * Experience working in controlled or regulated environments * Ability to identify and respond to deviations or unexpected situations during production * Basic knowledge of production equipment preparation and operation * Strong communication and teamwork skills. **Desirable Requirements:** * Experience in pharmaceutical or sterile manufacturing environments * Knowledge of controlled environments and contamination prevention practices **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 Technical Operations Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No