QC Validation Analyst (Pharmaceutical)

Location: Latina, Italy

Gross annual salary: EUR 24,000–36,000 basic salary; variable compensation is detailed in the offer.

Company

Independent technology consulting firm providing technical and functional solutions to businesses across information systems, telecom, life sciences, and engineering.

What you will do

• Perform chemical analyses using HPLC and Empower3 software.
• Execute and document QC testing in compliance with GMP guidelines.
• Design and perform validation protocols for HPLC, GC, and UV-Vis analytical methods.
• Evaluate accuracy, precision, specificity, linearity, range, detection and quantitation limits, robustness, and system suitability.
• Prepare and review validation protocols, reports, and risk assessments.
• Support method transfer and verification between laboratories or from R&D to QC while collaborating with cross-functional teams.

Requirements

• 2–3 years of experience with HPLC analysis using Empower3.
• Experience with analytical method validation in a GMP-regulated chemistry laboratory.
• Knowledge of cGMP and QC laboratory procedures in the pharmaceutical industry.
• Degree in Chemistry, Pharmaceutical Chemistry and Technology, or a related field.
• Fluent Italian and good command of English required.
• Ability to work precisely and efficiently in a regulated environment.

Culture & Benefits

• International community with more than 110 nationalities.
• Internal Academy with more than 250 training modules.
• Career development opportunities in a growing consulting organization.
• Regular internal events, including afterworks and team-building activities.
• Commitment to CSR through the WeCare Together program.

Hiring process

• Brief virtual or phone call.
• Approximately three interviews, depending on seniority.
• Possible case study, technical assessment, role play, or problem-solving exercise.