QC Validation analyst
Pubblicato il 12-08-2026 - Amaris Consulting in Latina
Job Description
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Join our team as QC Validation Analyst 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 an industrial 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
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- Perform chemical analysis using HPLC with Empower3 software
- Execute and document QC testing activities in compliance with GMP guidelines
- Design and execute validation protocols for analytical methods (e.g., HPLC, GC, UV-Vis)
in compliance with ICH and GMP guidelines
- Perform validation experiments to assess accuracy, precision, specificity, linearity, range, detection and quantitation limits, robustness, and system suitability
- Prepare and review validation documentation, including protocols, reports, and risk assessments
- Support method transfer and verification activities between laboratories or from R&D; to QC
- Collaborate with cross-functional teams to ensure product quality compliance
Your profile
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- 2-3 years of experience with HPLC analysis using Empower3 software
- Knowledge of cGMP and QC laboratory procedures in the pharmaceutical industry
- Academic background: Degree in Chemistry, Pharmaceutical Chemistry and Technology or related field
- Experience in analytical method validation in a GMP-regulated chemistry laboratory
- Fluent Italian and good command of English
- You have an ability to work prec