Executive Direttore, Quality Site Head Stein — Lonza
- Località
- Root
- Contratto
- full-time
- Pubblicato
- Ieri
Panoramica
Today, Lonza is a global leader in life sciences operating across five continents.
While we work in science, there’s no magic formula to how we do it.
Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people.
- Today, Lonza is a global leader in life sciences operating across five continents.
- While we work in science, there’s no magic formula to how we do it.
- Key Responsibilities: Quality Leadership & Site Governance
- Serve as the senior quality leader for the site and a trusted advisor to the Site Head and leadership team.
Responsabilità principali
- Key Responsibilities: Quality Leadership & Site Governance
- Serve as the senior quality leader for the site and a trusted advisor to the Site Head and leadership team.
- Define and execute the site's quality strategy in alignment with global quality objectives and business priorities.
- Lead all Quality functions, including Quality Assurance, Quality Control, Compliance, Validation, and Quality Systems.
- Foster a proactive quality culture that promotes accountability, continuous improvement, and patient-centric decision-making.
Processo di candidatura
- science- and risk-based approaches to quality oversight and decision-making.
- Anticipate and proactively mitigate quality and compliance risks associated with site growth, new technologies, and customer programs.
- Ensure effective escalation and resolution of critical quality issues while balancing patient safety, compliance, and business objectives. Customer & Stakeholder Engagement
- Build strong partnerships with customers, serving as a key quality representative for strategic client relationships.
- Collaborate closely with other site quality leaders and global quality teams to harmonize standards, processes, and best practices.
- Support business development activities, customer visits, due diligence assessments, and new product introductions.
- Represent the site within global quality networks and industry forums. Industry & Regulatory Leadership
- Monitor emerging regulatory requirements, industry trends, and technological advancements impacting Drug Product manufacturing.
Azienda e contesto
- As the organization expands its Drug Product (DP) manufacturing capabilities and scales operations, this role will provide strategic and operational quality leadership to ensure the highest standards of product quality, patient safety, regulatory compliance, and business performance.
- The Quality Site Head will drive the site's quality culture, strengthen organizational capabilities, and ensure alignment with global quality strategies while supporting the successful growth of a world-class Contract Development and Manufacturing Organization (CDMO).
- The role will play a critical part in preparing the site for future expansion, regulatory inspections, customer audits, and increasing manufacturing complexity.
- Build and develop a high-performing quality organization capable of supporting significant site growth and increasing operational complexity. Drug Product Quality Leadership
- Lead and strengthen all quality activities related to Drug Product manufacturing, packaging, testing, release, and lifecycle management.
- Ensure compliance with current GxP requirements, FDA, EMA, Swissmedic, and other applicable global regulatory standards.
- Provide expert guidance on quality aspects of aseptic processing, sterile manufacturing, biologics, and advanced Drug Product technologies, as applicable.
- Partner closely with Manufacturing, MSAT, Engineering, Supply Chain, and Technical Services to ensure robust quality oversight throughout the product lifecycle.
- Spend time on the shopfloor in Gemba's acting as a coach.
- Organizational Growth & Capability Development
Dettagli ulteriori
- We are looking for an Executive Director, Quality Site Head, Stein. Key Responsibilities: Quality Leadership & Site Governance
- Build and develop a high-performing quality organization capable of supporting significant site growth and increasing operational complexity. Drug Product Quality Leadership
- Ensure timely and effective investigation, root cause analysis, and implementation of corrective and preventive actions (CAPAs). Quality Systems & Continuous Improvement
- Establish and monitor meaningful quality performance indicators to drive operational excellence and business performance. Risk Management & Decision Making
- Apply science- and risk-based approaches to quality oversight and decision-making.
- Ensure effective escalation and resolution of critical quality issues while balancing patient safety, compliance, and business objectives. Customer & Stakeholder Engagement
- Represent the site within global quality networks and industry forums. Industry & Regulatory Leadership
- Act as a visible leader internally and externally, representing Lonza at industry, regulatory, and community levels. Key Requirements and Qualifications
Note e contenuto originale
- We are looking for an Executive Director, Quality Site Head, Stein.
- Role Purpose:
- Key Responsibilities:
- Quality Leadership & Site Governance
- Build and develop a high-performing quality organization capable of supporting significant site growth and increasing operational complexity.
- Drug Product Quality Leadership
- Ensure timely and effective investigation, root cause analysis, and implementation of corrective and preventive actions (CAPAs).
- Quality Systems & Continuous Improvement
- Establish and monitor meaningful quality performance indicators to drive operational excellence and business performance.
- Risk Management & Decision Making
Domande frequenti su questo annuncio
Che stipendio offre Lonza per questa posizione?
Lonza indica CHF 85'500 - 129'500 lordi annui per questo ruolo a Root. Questo è lo stipendio pubblicato nell'annuncio originale (o, quando il datore non specifica una cifra, una stima realistica per ruolo e settore) — il calcolatore di questo sito lo converte nel netto reale una volta applicate imposta da frontaliere e contributi sociali.
È un ruolo a tempo pieno, e che tipo di contratto offre Lonza?
Questo annuncio è una posizione a tempo pieno. Il tipo di contratto mostrato qui arriva direttamente dall'annuncio originale del datore di lavoro; conferma sempre orario esatto, preavviso e durata del periodo di prova con Lonza durante il colloquio, perché questi dettagli possono variare anche all'interno della stessa categoria contrattuale.
Serve un permesso da frontaliere per un ruolo nel canton Lucerna?
I residenti UE/AELS nella zona di frontiera del paese confinante con il canton Lucerna possono richiedere il Permesso G; il datore di lavoro svizzero lo presenta all'ufficio della migrazione di quel canton dopo la firma del contratto. Regole sulla zona di frontiera e tempi di lavorazione variano per paese confinante e canton — verifica i dettagli con l'ufficio della migrazione del canton Lucerna o con HR durante il colloquio.
Come mi candido a questa posizione presso Lonza?
Usa il pulsante "Candidati ora" in questa pagina — rimanda direttamente all'annuncio originale di Lonza su lonza.wd3.myworkdayjobs.com, quindi la tua candidatura arriva direttamente nel sistema di gestione candidature del datore di lavoro. Frontaliere Ticino non raccoglie né inoltra candidature in proprio.
