23 set - Bardi
Jazz Pharmaceuticals
Overview
In this role, you will perform quality control testing and support sampling across finished products, APIs, and materials within a GMP framework. You will ensure data integrity, proper lab practices, and compliant documentation to uphold product quality. You'll collaborate with cross-functional teams to drive validation activities and continuous improvement within QC. This position offers hands-on work in analytical methods and equipment qualification in a global, patient-focused company.
Retribuzione / Benefits
total compensation package
discretionary annual cash premio or incentive compensation
discretionary equity grants
Global Cash Bonus Plan
Long Term Equity Incentive Plan
Responsabilità
Perform analytical QC testing following validated procedures and training plans
Support sampling of finished products, APIs, intermediates, starting materials, and packaging components
Ensure data accuracy, traceability, and compliant contemporaneous recording
Qualify and maintain lab equipment and refer to approved procedures
Prepare and review SOPs, method validation, equipment qualification, and stability documentation
Participate in analytical validation, cleaning validation,
and stability studies protocols/reports
Investigate quality deviations and escalate to QA/line manager
Ensure compliance with GMP, Environmental, Health and Safety policies, and company Codes of Conduct
Contribute to continuous improvement initiatives within the Operational Excellence culture
Attend training on GMP/QMS procedures and Integrated Management System
Requisiti fondamentali
Two or more years in a Pharmaceutical Quality Control laboratory
Experience in analytical method validation (protocol, execution, report)
Experience with QC equipment: HPLC, UPLC, TOC, automatic titrators
Proficient with QC software: Empower 3 CDS, Chromeleon, LabX, TiAMO, OpenLab
Experience in sampling/testing for Cleaning Validation/Verification, APIs, raw materials
Drafting/reviewing SOPs and technical documents in Italian and English
Good English (written and spoken)
Teamwork and multi-project capability
Experience with 6S in QC laboratory
Team building
clear communication
collaboration across functions
HPLC/UPLC
TOC
automatic titrators
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