GMP Quality Assurance Associate (Entry Level)

ACS Dobfar S.p.A.; Tribiano; On-site; EUR 32,000 - 42,000; Full time

Job summary

ACS Dobfar S.p.A. is seeking a Quality Assurance Employee to assist in GMP quality events, document management, and QA documentation preparation. The role involves data entry, organizing change-related records, and supporting SOP development, training verification, and regulatory readiness.

The candidate should have basic GMP knowledge, familiarity with data integrity, and good attention to detail. Italian fluency and professional English are preferred, with entry-level experience in pharma

Qualifications

• Degree or Diploma in a chemical/pharmaceutical field.
• Experience in GMP environments is preferred but not required.
• Familiarity with GMP documentation and QA processes is beneficial.

Responsibilities

• Supports GMP quality events management (changes, complaints, deviations, CAPAs) via electronic document system.
• Collects and organizes supporting documentation for change requests, complaints, deviations, and CAPAs.
• Monitors GMP compliance activities and reports discrepancies to QA supervisors.
• Assists in preparing GMP documents including risk assessments and validation reports.
• Supports drafting and updating SOPs and other quality documents.
• Verifies training records and monitors qualification status.
• Verifies alarms/events in SCADA and reports issues to QA.

Skills

Attention to detail

Teamworking

Organizational skills

Willingness to learn GMP

Reliability and accountability

Education

Degree in Chemistry, Chemistry and Pharmaceutical Technology (CTF), Pharmacy, Biology or related scientific disciplines

Diploma from an Industrial Technical Institute with specialization in Chemistry

Tools

Microsoft Office tools

Electronic document management systems

SCADA systems

SAP or similar ERP systems

Job description

ACS Dobfar S.p.A. is seeking a Quality Assurance Employee to assist in GMP quality events, document management, and QA documentation preparation. The role involves data entry, organizing change-related records, and supporting SOP development, training verification, and regulatory readiness.

The candidate should have basic GMP knowledge, familiarity with data integrity, and good attention to detail. Italian fluency and professional English are preferred, with entry-level experience in pharma