Job vacancies on Sidel.com Parma Aseptic Field Commissioning Engineer Automation (Filler) YOUR OPPORTUNITY Take the lead on deploying and optimizing Sidel’s advanced equipment at customer sites worldwide. Drive start-ups, troubleshoot complex systems, and support aseptic prototype qualifications—all while
Position Description: We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and
_ The IMA Group is a world leader in the design and manufacture of automatic machines for the processing and packaging of pharmaceutical, cosmetic, food, tea and coffee products as well as in the automation of industrial
Tipo Lavoro: Dipendente Tipologia Contratto: Tempo indeterminato Località: milano, IT Chi siamo Chiesi è un gruppo biofarmaceutico internazionale focalizzato sulla ricerca, con 90 anni di esperienza e presente in oltre 30 Paesi, con sede centrale a
SummaryLocation: Ivrea, Italy (onsite)Role PurposeDuring the pilot plant ramp‑up and operationalization, support line unit efforts in developing compliant manufacturing and QC‑related quality systems, focusing on master batch records, logbooks, forms, and procedures. Oversee initial validation activities
Philogen S.p.A. is looking for a “ GMP Sterility Assurance Specialist/Expert ” who will report to the GMP Quality Assurance Manager and contribute to the definition, implementation, and verification of Contamination Control strategies, ensuring compliance with
Position Description: We are now seeking a CQV Engineer to join our growing operations in Italy. The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and
Location: Ivrea, Italy (Onsite)Role PurposeDuring the pilot plant ramp up and operationalization support line units efforts in developing compliant manufacturing and QC-related quality system, with particular focus on master batch records, logbooks, forms, procedures. Oversee the
Experteer OverviewAs a CQV Engineer in Italy, you will develop and execute documentation for commissioning, qualification, and validation of facilities, utilities, and equipment. You will write protocols, perform field verifications, and craft summary reports at client
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description When you’re part of the team at Thermo Fisher Scientific, you’ll do important work. You’ll have the opportunity to grow and learn in a culture that empowers your development. We have built an inclusive, global environment that
Experteer Overview In this role you will support the pilot plant ramp-up and establish a compliant manufacturing and QC quality system. You will oversee initial validation activities and QC PQs while coordinating the QA shopfloor team
Summary Location: Ivrea, Italy (onsite) Role Purpose During the pilot plant ramp‑up and operationalization, support line unit efforts in developing compliant manufacturing and QC‑related quality systems, focusing on master batch records, logbooks, forms, and procedures. Oversee
Location: Ivrea, Italy (Onsite) Role Purpose During the pilot plant ramp up and operationalization support line units efforts in developing compliant manufacturing and QC-related quality system, with particular focus on master batch records, logbooks, forms, procedures.
Job Description Job Summary As a Maintenance Engineer at Tetra Pak , you’ll take on more responsibility in maintaining and installing Tetra Pak equipment. You’ll work closely with customers and internal teams, gaining valuable experience while
Philogen S.p.A. is looking for a “GMP Sterility Assurance Specialist/Expert ” who will report to the GMP Quality Assurance Manager and contribute to the definition, implementation, and verification of Contamination Control strategies, ensuring compliance with applicable