Quality Assurance Pharma
Pubblicato il 22-09-2026 - Amaris Consulting in Latina
Who are we?Join our team 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.
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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 deviation management and CAPA processes.
- Academic background: Master’s degree in Pharmacy, Biotechnology, Chemistry, or related field.
- Fluent Italian and English.
- You have strong organizational and analytical skills with attention to detail.
- You are able to adapt quickly, work in a team and maintain high-quality stand