Life Science Consultant, Supply Chain

Job Post has been updated successfully Job Share Recipient Email Job Description Share Share Email Facebook Twitter Linkedin AddThis Sharing ButtonsShare to FacebookFacebookShare to TwitterTwitterShare to PrintPrintShare to EmailEmailShare to MoreAddThis Print Life Science Consultant, Supply Chain (Turin, 10024), Piedmont - Italy | Posted - 24/04/23 Overview 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  Life Science Consultant, Supply Chain Location:  Ivrea,Italy Start Date: As soon as Possible We are a consultancy firm with a focus on the life science industry, dedicated to providing custom solutions to pharmaceutical companies worldwide. 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) Reviewing 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 enviornment Able to manage multiple tasks and work to tight deadlines Creative, structured, open-minded for new ideas, and agile drive Soft Skills Strong organisational 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.