Onsite Quality Compliance

Amaris Consulting is hiring a GMP Materials & Compliance Specialist in Latina for a fully onsite role in the Life Sciences sector. You will manage GMP material master data, assess compliance, and support QA/QC teams while maintaining SAP records and supporting regulatory alignment.Ideal candidates hold a science degree and have GMP experience, with strong...

Amaris Consulting is hiring a GMP Materials & Compliance Specialist for an onsite role in Latina.Tutti i candidati sono invitati a leggere attentamente la seguente descrizione del lavoro e le relative informazioni prima di candidarsi.You will manage GMP material master data, assess compliance, and support QA/QC in material disposition.Collaboration with...

Would you like to start a new professional adventure as a Quality Compliance & LIMS Specialist in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ?Define and maintain analytical specifications in the LIMS for GMP raw materials, intermediates and manufactured products.Work with QC, QA, Manufacturing and client teams to...

Overview In this role you will lead and optimize the Quality Management System to ensure GMP, FDA and EU compliance across the site. You will partner with cross-functional teams to drive quality improvements, manage inspections, training, and documentation, and report on QMS performance. You will enable a culture of quality and continuous improvement,...

Would you like to start a new professional adventure as a Quality Compliance & LIMS Specialist in one of our opportunities in the Life Sciences industry in Latina (fully onsite position) ?Define and maintain analytical specifications in the LIMS for GMP raw materials, intermediates and manufactured products.Work with QC, QA, Manufacturing and client teams to...

Overview In this role you will lead and optimize the Quality Management System to ensure GMP, FDA and EU compliance across the site. You will partner with cross-functional teams to drive quality improvements, manage inspections, training, and documentation, and report on QMS performance. You will enable a culture of quality and continuous improvement,...

pWould you like to start a new professional adventure as a bRegulatory Affairs Consultant /b in one of our opportunities in the bLife Sciences /b industry in bLatina (fully onsite position) ? /b /p ul liDraft and review Quality and CMC sections of regulatory dossiers, with a focus on Module 3 of the CTD. /li liPrepare and update pharmaceutical quality...

\"It is the people who make Demont great every day\". Junior Nuclear Engineer - Quality & Compliance * Reporting to: Quality / IMS Work location: Millesimo (SV), with possible business travels in Italy and abroad Job Description Job ID D26_07 Contract Type Temporary/Permanent – Full-time About Us Demont, founded in 1972, is a vertically integrated EPC...

Overview In this role you will lead and optimize the Quality Management System to ensure GMP, FDA and EU compliance across the site. You will partner with cross-functional teams to drive quality improvements, manage inspections, training, and documentation, and report on QMS performance. You will enable a culture of quality and continuous improvement,...