Descrizione dell'offerta
Quality Assurance Associate – Filling Cartridges
In this QA Associate role at Lilly’s Sesto Fiorentino site, you ensure cGMP compliance and quality across the cartridge filling area. You act as the primary quality escalation point and partner with cross-functional teams to support the new formulation suite from early stages. You contribute to regulatory readiness, inspections, and a strong Quality culture, shaping robust quality systems at scale. This position offers meaningful impact on patient outcomes through disciplined quality and collaboration. Serve as the accountable escalation point for quality issues in the production area Ensure consistent application of cGMP standards and Lilly quality requirements across the area Support preparation for regulatory inspections and contribute to the site self-inspection program Investigate deviations in the Cartridge area and perform Quality Assessments in Veeva QMS Review and approve qualification protocols and procedures Act as Media Fill observer and approve work orders where applicable Actively contribute to site Quality Systems and Quality Culture initiatives Master's Degree in a Scientific discipline 1-2 years of experience in pharmaceutical industry operations Solid knowledge of current GMPs, pharmaceutical legislation, and regulatory requirements Good command of English (minimum B2 CEFR level) Strong communication and influencing skills Collaborative mindset with a pragmatic, compliance-oriented approach In this QA Associate role at Lilly’s Sesto Fiorentino site, you ensure cGMP compliance and quality across the cartridge filling area. You ac… #J-18808-Ljbffr
In this QA Associate role at Lilly’s Sesto Fiorentino site, you ensure cGMP compliance and quality across the cartridge filling area. You act as the primary quality escalation point and partner with cross-functional teams to support the new formulation suite from early stages. You contribute to regulatory readiness, inspections, and a strong Quality culture, shaping robust quality systems at scale. This position offers meaningful impact on patient outcomes through disciplined quality and collaboration. Serve as the accountable escalation point for quality issues in the production area Ensure consistent application of cGMP standards and Lilly quality requirements across the area Support preparation for regulatory inspections and contribute to the site self-inspection program Investigate deviations in the Cartridge area and perform Quality Assessments in Veeva QMS Review and approve qualification protocols and procedures Act as Media Fill observer and approve work orders where applicable Actively contribute to site Quality Systems and Quality Culture initiatives Master's Degree in a Scientific discipline 1-2 years of experience in pharmaceutical industry operations Solid knowledge of current GMPs, pharmaceutical legislation, and regulatory requirements Good command of English (minimum B2 CEFR level) Strong communication and influencing skills Collaborative mindset with a pragmatic, compliance-oriented approach In this QA Associate role at Lilly’s Sesto Fiorentino site, you ensure cGMP compliance and quality across the cartridge filling area. You ac… #J-18808-Ljbffr
Candidatura e Ritorno (in fondo)
Ricevi annunci simili
Inserisci la tua email: ti avvisiamo quando escono nuovi annunci corrispondenti.
✅ Controlla la tua email e clicca il link per confermare l'alert.
Nessun account necessario. Disiscrizione con un clic dall'email.