Pharma QA Deviation Specialist | GMP, CAPA & Compliance

Amaris Consulting | Part of Mantu; Lazio; On-site; EUR 24,000 - 36,000; Full time

Benefits offered by this job

International community

Academy training

Team events

CSR programs

Job summary

Amaris Consulting is seeking a Quality Assurance professional in Latina to ensure GMP-compliant pharmaceutical products and documentation across production, R&D and supply chain teams.

You will review batch records, SOPs and quality manuals while conducting deviation analysis, CAPA and audits preparation. English and Italian fluency, plus 2+ years in QA, are required to join our international environment.

Qualifications

• 2+ years QA experience in the pharmaceutical industry (sterile environment).
• Knowledge of GMP guidelines and pharmaceutical regulatory standards.
• Experience with deviation management and CAPA processes.
• Academic background: Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field.
• Fluent Italian and English.
• Strong organizational and analytical skills with attention to detail.
• Able to adapt quickly, work in a team and maintain high-quality standards.

Responsibilities

• Ensure compliance of pharmaceutical products with GMP and regulatory standards.
• Perform document review and approval (batch records, SOPs, quality manuals).
• Conduct deviation analysis, CAPA implementation and monitoring.
• Support audits and regulatory inspections by preparing documentation and answering queries.
• Collaborate with production, R&D and supply chain teams to guarantee quality across processes.
• Perform risk assessments and contribute to continuous improvement projects.
• Provide training to colleagues on quality procedures and regulatory updates.
• Prepare and present reports on quality indicators and project progress.

Skills

Quality Assurance

GMP knowledge

Analytical skills

Teamwork

Attention to detail

Education

Master’s degree in Pharmacy

Biotechnology

Chemistry

Related field

Job description

Amaris Consulting is seeking a Quality Assurance professional in Latina to ensure GMP-compliant pharmaceutical products and documentation across production, R&D and supply chain teams.

You will review batch records, SOPs and quality manuals while conducting deviation analysis, CAPA and audits preparation. English and Italian fluency, plus 2+ years in QA, are required to join our international environment.