Pharma QA Deviation Specialist | CAPA & GMP

Amaris Consulting | Part of Mantu

Latina

On-site

EUR 24,000 - 36,000

Full time

3 days ago
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Benefits offered by this job

International community
Internal Academy training
Team events
CSR program

Job summary

Amaris Consulting | Part of Mantu in Latina is seeking a Quality Assurance professional to ensure GMP compliance and support regulatory inspections in a dynamic pharmaceutical environment.

You will review batch records, SOPs, and quality manuals, perform deviation analyses, and implement CAPA while collaborating with production, R&D and supply chain teams to safeguard product quality and drive continuous improvement.

Qualifications

  • At least 2 years of QA experience in the pharmaceutical industry (sterile).
  • Knowledge of GMP guidelines and regulatory standards.
  • Experience with deviation management and CAPA processes.
  • 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 GMP compliance of pharmaceutical products.
  • Review and approve batch records, SOPs, and quality manuals.
  • Conduct deviation analysis and implement CAPA.
  • Support audits and regulatory inspections.
  • Collaborate with production, R&D and supply chain to ensure quality.
  • Perform risk assessments and drive continuous improvement.
  • Provide training on quality procedures and regulatory updates.
  • Prepare and present quality indicators and project progress reports.

Skills

GMP Knowledge
Deviation management
CAPA processes
Regulatory standards
Analytical skills
Interpersonal skills

Education

Master's in Pharmacy

Job description

Amaris Consulting | Part of Mantu in Latina is seeking a Quality Assurance professional to ensure GMP compliance and support regulatory inspections in a dynamic pharmaceutical environment.

You will review batch records, SOPs, and quality manuals, perform deviation analyses, and implement CAPA while collaborating with production, R&D and supply chain teams to safeguard product quality and drive continuous improvement.

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