Scientist Quality Control
Pubblicato il 22-09-2026 - Jazz Pharmaceuticals in Villa guardia
Overview
As a Scientist Quality Control, you ensure analytical QC testing aligns with GMP and approved procedures within Gentium Srl. You play a key role in sampling, data integrity, and validation activities to support a robust QC program. You collaborate across the QA and production teams to sustain quality, safety, and compliance. This role offers impact at the intersection of science and patient care, within a global biopharma context.
Retribuzione / Benefits
- total compensation packages
- discretionary annual cash premio or incentive compensation
- discretionary equity grants
- market-competitive pay
- career development opportunities
Responsabilità
- Perform analytical QC testing per written instructions and training plan
- Sample finished products, APIs, intermediates, starting materials, raw materials, packaging components, in-process control and cleaning validation samples per approved instructions
- Apply QC and site procedures; report deviations to line manager/QA
- Review analytical results and ensure data accuracy, traceability and integrity
- Maintain lab and equipment cleanliness and qualification per instructions with safety and quality focus
- Ensure reagents and standards are available, non-expired, and properly recorded in systems
- Confirm correct labeling and storage of reagents, standards and samples
- Participate in analytical validation, cleaning validation, and stability studies protocols/reports
- Assist in quality deviation investigations as required
- Draft QC lab instructions (SOPs, method validation protocols/reports, equipment qualification)
- Engage in Continuous Improvements via Operational Excellence culture
- Monitor compliance with GMP and Quality System within area of responsibility
- Follow EH&S; procedures under the Integrated Management System
- Attend training on Integrated Management System, GMP Quality, Procedures and protocols
- Perform work in accordance with Legislative Decree 81/08 and company policies
- Support compli