Entry-Level Pharma QA: GMP

An innovative consulting firm based in Latina, Italy, is seeking a Quality Assurance Specialist to ensure compliance with GMP and regulatory standards in the pharmaceutical field. This entry-level role involves document review, audits preparation, and supporting quality processes across projects. Candidates should have a Master's degree and a minimum of 6...

Johnson & Johnsonis seeking a Quality Assurance Associate for the Borgo San Michele (Latina) site. The role is a 12-month fixed-term contract within the Quality department, ensuring product conformance to GMP and national/international standards.You will review production data, manage quality issues, and support cross-functional investigations. Requirements...

Johnson & Johnsonis seeking a Quality Assurance Associate for the Borgo San Michele (Latina) site. The role is a 12-month fixed-term contract within the Quality department, ensuring product conformance to GMP and national/international standards.You will review production data, manage quality issues, and support cross-functional investigations. Requirements...

Johnson & Johnsonis seeking a Quality Assurance Associate for the Borgo San Michele (Latina) site. The role is a 12-month fixed-term contract within the Quality department, ensuring product conformance to GMP and national/international standards.You will review production data, manage quality issues, and support cross-functional investigations. Requirements...

Johnson & Johnsonis seeking a Quality Assurance Associate for the Borgo San Michele (Latina) site. The role is a 12-month fixed-term contract within the Quality department, ensuring product conformance to GMP and national/international standards.You will review production data, manage quality issues, and support cross-functional investigations. Requirements...

Who are we?Join our team and start a new adventure in an international and dynamic environment where you will be able to fulfil your career expectations in a fast-growing organization.Being a consultant at Amaris Consulting means positioning yourself as a technical and functional expert in the pharmaceutical field, but above all being an ambassador of our...

S.T.B. ValiTech S.r.l., società di consulenza specializzata nel settore Life Science, ricerca Validation & Qualification Engineer da inserire in progetti GMP in ambito farmaceutico, chimico e biotech. La risorsa sarà coinvolta in attività di commissioning, qualification e convalida di impianti, equipment di processo, clean utilities e sistemi di...

Who are we?Join our team and start a new adventure in an international and dynamic environment where you will be able to fulfil your career expectations in a fast-growing organization.Being a consultant at Amaris Consulting means positioning yourself as a technical and functional expert in the pharmaceutical field, but above all being an ambassador of our...

A prestigious company operating in the Pharma / Life Sciences sector has entrusted us with the search for a: PART-TIME CONTRACT DURATION: 18–24 months START DATE: May 2026 Do you have experience managing complex changes in highly regulated Pharma capital projects? Would you like to play a key role in controlling time, costs and risks within GMP...