342823BR
Apr 05, 2022
Spain
Job Description
Job Purpose
- Coordinate finished products label and package activities.
- Perform the production activities in accordance with the GMP requirements in observance of documentation for production and internal SOPs
Major Accountabilities
• Manage supply chain of all raw material through an ERP system
• Stock management and control (including FEFO system, purchase order supervision etc)
• Manage restocking in collaboration with external wharehouse
• Prepare raw materials prior to batch manufacturing
• Coordinate finished products labelling and packaging
• Execute labelling and packaging of products
• Responsible for the control of Raw Materials (MP) for the manufacturing of the sterile batch (e.g. labels, shelf-life, compliance with BR)
• Execute production activities in Class C, D and unclassified areas, according the Batch Record instructions, aseptic behavior instructions and SOPs
• Set up the equipment for labelling and packaging activities and for production activities performed in class D and unclassified areas
• Observe behavioral standards and flow of materials in the areas with controlled contamination (and with particular regard to the sterile room) in compliance with the internal procedures
• Keep track in a timely manner of all the activities performed during the manufacturing process, as per Data Integrity and SOPs instruction
• Address promptly any unexpected situations (e.g. air pressure decay, temperature or humidity change, machine stop) or deviations from the validated standard operations
Although this is a shift job (nights from 10 p.m. to 6 a.m. and mornings from 6 a.m. to 2 p.m.), we offer a permanent contract, extensive training and professional stability.
- Coordinate finished products label and package activities.
- Perform the production activities in accordance with the GMP requirements in observance of documentation for production and internal SOPs
Major Accountabilities
• Manage supply chain of all raw material through an ERP system
• Stock management and control (including FEFO system, purchase order supervision etc)
• Manage restocking in collaboration with external wharehouse
• Prepare raw materials prior to batch manufacturing
• Coordinate finished products labelling and packaging
• Execute labelling and packaging of products
• Responsible for the control of Raw Materials (MP) for the manufacturing of the sterile batch (e.g. labels, shelf-life, compliance with BR)
• Execute production activities in Class C, D and unclassified areas, according the Batch Record instructions, aseptic behavior instructions and SOPs
• Set up the equipment for labelling and packaging activities and for production activities performed in class D and unclassified areas
• Observe behavioral standards and flow of materials in the areas with controlled contamination (and with particular regard to the sterile room) in compliance with the internal procedures
• Keep track in a timely manner of all the activities performed during the manufacturing process, as per Data Integrity and SOPs instruction
• Address promptly any unexpected situations (e.g. air pressure decay, temperature or humidity change, machine stop) or deviations from the validated standard operations
Although this is a shift job (nights from 10 p.m. to 6 a.m. and mornings from 6 a.m. to 2 p.m.), we offer a permanent contract, extensive training and professional stability.
Diversity & Inclusion / EEO
Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
Minimum Requirements
- Education: Technical high school
- Languages: Basic English knowledge
- Experiences: It would be preferable a previous working experience in the pharmaceutical industry
- Languages: Basic English knowledge
- Experiences: It would be preferable a previous working experience in the pharmaceutical industry
ONCOLOGY
ADVANCED ACCELERATOR APPLICATIONS
Spain
Zaragoza
AAA Ibérica S.L.U.
Technical Operations
Full Time
Regular
No
