Quality Control Technician

Siemens Healthineers Radiopharma – Manufacturing – Professional Senior At Siemens Healthineers (SHS) Radiopharma, we are committed to driving sustainable progress through cutting-edge technology.We empower our customers by bridging the physical and digital worlds—enhancing the way we live, work, and move, today and for future generations.We believe that business success begins with our people.That's why we prioritize a culture where individuals thrive.Our diverse team is ready to support, inspire, and challenge you to grow in new and meaningful ways.Together, there are limitless possibilities of where our shared journey may lead.As the global leader in the supply of positron emission tomography (PET) radiopharmaceuticals, SHS Radiopharma pioneered the commercial PET radiopharmacy model over 30 years ago—and continues to shape the future of molecular imaging.Join us as a Quality Control Technician, based in Colleretto Giacosa (TO), Italy and help us shape the future of precision theranostics while advancing patient care.Your responsibility within the Quality Control Laboratory will be to ensure analytical activities, processes, and equipment comply with established quality standards, internal procedures, and applicable regulatory requirements.Your role:Perform batch analysis in accordance with approved Standard Operating Procedures (SOPs)Prepare all solutions, reagents, standards, and materials required for routine laboratory activitiesCollaborate with the Quality Control Manager in the implementation and follow-up of Corrective and Preventive Actions (CAPA) related to Quality Control processes, equipment, and laboratory areas.Support specialized external personnel during maintenance, calibration, qualification, and validation activitiesExecute calibration, verification, qualification, and validation activities of Quality Control processes and equipment in compliance with SOPs and regulatory standardsThe position involves rotating morning and night shifts.Your expertise:Technical diploma or degree in Chemistry, Biology, pharmaceutical sciences or any related fieldMinimum 1-3 years' experience in Quality Control or Analytical laboratory roles within GMP-regulated environments.Previous experience in radiopharmaceutical companies is a plus.Local language and English (both written and spoken)Who we are:We are a team of more than 73,000 highly dedicated Healthineers in more than 70 countries.As a leader in medical technology, we constantly push the boundaries to create better outcomes and experiences for patients, no matter where they live or what health issues they are facing.Our portfolio is crucial for clinical decision-making and treatment pathways.How we work:When you join Siemens Healthineers, you become one in a global team of scientists, clinicians, developers, researchers, professionals, and skilled specialists, who believe in each individual's potential to contribute with diverse ideas.We are from different backgrounds, cultures, religions, political and/or sexual orientations, and work together, to fight the world's most threatening diseases and enable access to care, united by one purpose: to pioneer breakthroughs in healthcare.For everyone.Everywhere.Sustainably.Check our Careers Site at Jobs at Siemens Healthineers AGAs an equal opportunity employer, we welcome applications from individuals with disabilities.We care about your data privacy and take compliance with GDPR as well as other data protection legislation seriously.For this reason, we ask you not to send us your CV or resume by email.Please create a profile within our talent community and subscribe to personalized job alert that will keep you posted about new opportunities.To all recruitment agencies: Siemens Healthineers' recruitment is internally managed, with external support permitted only when a qualified supplier has established a formal contract with us.Unsolicited candidate submissions and referrals, absent a current supplier contract, do not establish consent and are ineligible for fees.We delete and destroy unsolicited information, thus, would recommend you refrain from any such practices.Your adherence to our policies is appreciated.#J-*****-Ljbffr