Onsite GMP Materials & Compliance Specialist – Latina

Amaris Consulting | Part of Mantu; Latina; Presencial; EUR 24.000 - 36.000; Tempo integral

Benefícios oferecidos por esta vaga

Meal vouchers

Health insurance

Flexible working

Resumo da vaga

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 SAP knowledge and fluency in English; Italian/C2 is preferred.

Qualificações

• Degree in Pharmaceutical Chemistry and Technology, Pharmacy, Chemistry, Biotechnology or a related scientific field, or equivalent experience.
• Good knowledge of SAP, with previous experience managing material master data considered an advantage.
• Knowledge of EU-GMP, 21 CFR Part 210 and 211, ICH guidelines and relevant Pharmacopoeias.

Responsabilidades

• Manage GMP material master data for purchased materials and products.
• Assess material compliance for the intended use in line with procedures and regulations.
• Review and maintain material information required for GMP activities, quality controls and material disposition.
• Work with suppliers to resolve material master data issues identified during inspections or testing.
• Support Quality Control and Quality Assurance teams in review and disposition of materials.
• Ensure material records in SAP are accurate, complete and up to date.
• Prepare product safety risk assessments when required.
• Maintain clear documentation and updates to material-related procedures and records.

Conhecimentos

GMP materials management

SAP knowledge

Quality/compliance experience

Formação

Science degree (Pharmaceutical Chemistry/Pharmacy/ Chemistry/Biotechnology)

Ferramentas

SAP

Descrição da vaga

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 SAP knowledge and fluency in English; Italian/C2 is preferred.