Social network you want to login/join with: Life Science Consultant, Supply Chain, Turin Client: Advanced Accelerator Applications AAA a Novartis Company Location: Ivrea, Italy Job Category: Consulting EU work permit required: Yes Job Reference: Job Views: 10 Posted: 20.02.2025 Expiry Date: 06.04.2025 Job Description: We are looking for enthusiasts KVALITO Consulting Group is a strategic partner and global Life Science network for regulated industries with a focus on quality. Headquartered in Basel, Switzerland, we have subsidiaries in Germany, the Czech Republic, Ireland, and Malaysia. With our enthusiasm for progressive technologies and our in-depth knowledge of industry best practices and regulations, we drive effective and efficient project delivery to keep our industry-leading clients ahead of the competition. Our leadership and consultants combine decades of experience in enterprise environments. To cover all essential technical areas in the field of digital and mobile, KVALITO works with reliable Technology Partners worldwide. For more information, please visit us at www.KVALITO.ch. Life Science Consultant, Supply Chain Location: Ivrea, Italy Start Date: As soon as Possible We are currently looking for a Supply Chain Consultant to join our team on a permanent basis to implement a cloud-based customized solution in Supply Chain for our client, a pharmaceutical company located in Ivrea, Italy. Major Accountabilities As a Supply Chain Consultant, you will serve as a SuperUser for the Supply Chain software implementation, working closely with stakeholders on site. Your main responsibilities will include: Business Validation Deliverables: Writing of User Requirement Specifications (URS), aligning with key stakeholders on site, reviewing Functional Specifications (FS), and executing Operational Qualification (OQ) and Performance Qualification (PQ). Data Management/Cleansing: Verification and alignment of Master data. Training: Training Key Users on site. Standard Operating Procedure (SOP) Writing. Leading communication: Between Key Users on site and IT. Minimum Qualifications and Experience Education: Master's degree in Science, Engineering, Operations, Pharmacy or equivalent. Language: Fluent in English – written & spoken. Native Italian speakers. Work Experience: Min. 2-3 years of working experience in a GMP environment (Supply Chain Operations) within the pharmaceutical industry. Experience working within a complex environment. Able to manage multiple tasks and work to tight deadlines. Creative, structured, open-minded for new ideas, and agile drive. Soft Skills: Strong organizational and time management skills. Able to work independently and as part of a team. Must have strong problem-solving skills. Attention to detail and accuracy. Quick learner, keen to learn new skills. We Offer Great Benefits: Flat hierarchies and responsibility from the beginning. People-oriented culture. Diversity and inclusion focused environment. Global client projects in a multinational environment. Flexible working hours and home-office. Involvement in global conferences. Individual professional development, training, and coaching. Unlimited full employment contract. Excellent remuneration package consisting of a competitive salary plus a substantial bonus. Contact: If you have the necessary background and experience and would like to join a small team responsible for a truly global operation, then please send your application to recruiting(at)kvalito.ch including your: CV, cover letter and supporting documents (i.e., diplomas, certificates, references). Availability - earliest start date. Salary expectations. Location preference. We are looking forward to your application. Your KVALITO Team. J-18808-Ljbffr