Do you enjoy working with cutting-edge technology? Would you like to help shape the future of our global energy? Join our Team! Partner with the best Responsible for Product quality review associated with the manufacturing process.
Role : Senior QA Automation Engineer (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Senior QA Automation Engineer to design, implement, and maintain automated testing frameworks for
PE Global Recruitment are currently recruiting for a Mechanical Construction Manager to join our client on a Data Centre project in Italy. This is a full time, permanent role based in Bertonico. The Job: This role
Location: Italy - San Giorgio di Nogaro (UD)Are you passionate about being part of a successful team? Are you excited by the prospect of working for an industry leader in Energy Technology?Join our team!Our Industry & Energy Technology
OUR STORY At STMicroelectronics, we believe in the power of technology to drive innovation and make a positive impact on people, businesses, and society. As a global semiconductor company, our advanced technologies and chips form the
Validation Specialist (Data & Compliance) Italy - Onsite - Other - Other - Permanent contract We are hiring a CSV Specialist in Florence, Italy. Specific activities and responsibilities: Plan, coordinate, and execute Computerized System and SW
OUR STORY At STMicroelectronics, we believe in the power of technology to drive innovation and make a positive impact on people, businesses, and society. As a global semiconductor company, our advanced technologies and chips form the
Process & Computer System Validation Specialist (GCP) Philogen S.p.A., a biotech company listed on the Milan Stock Exchange and a leader in the development of innovative anti‑tumor therapies, is looking for a highly motivated and qualified
Overview As Construction Manager, you oversee supplier activities across prefabrication, fabrication and module construction in Italy. You coordinate supplier and foreman teams to ensure safety, quality and on-time delivery, acting as the liaison among suppliers, contractors
Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional