QA Deviation Specialist – Sterile Manufacturing
Latina
Permanent Job
Join our team as Quality Assurance in Latina and start a new adventure in an international and dynamic environment where you will be able to fulfil your career expectations in a fast‑growing organization.
Being a consultant at Amaris Consulting means positioning yourself as a technical and functional expert in the pharmaceutical field, but above all being an ambassador of our organization to clients thanks to your interpersonal skills and ability to listen in order to build a strong relationship of trust with our clients and fully understand their challenges and issues. Your curiosity and eagerness to learn as we support over 1000 clients from all sectors worldwide.
Your missions
- 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.

Your profile
- Experience with Quality Assurance in the pharmaceutical industry (6 months minimum).
- Knowledge of GMP guidelines and pharmaceutical regulatory standards.
- Experience with root cause analysis, deviation management and CAPA processes with sterile products (mandatory).
- Academic background: Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field.
- Fluent Italian and English .
- Fully available for onsite work in Latina .
- You have strong organizational and analytical skills with attention to detail.
- You are able to adapt quickly, work in a team and m

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