QA Analytics Manager — GxP & Quality Compliance Lead

Lonza; Oberwallis; Vor Ort; Vertraulich; Vollzeit

Benefits dieser Stelle

Agile career and dynamic culture

Inclusive and ethical workplace

Compensation programs recognizing high

Benefits dependent on role and locale

Zusammenfassung

Lonza is seeking a QA Manager (f/m/d) within QA Analytics in Visp, Switzerland. You will ensure GxP compliance, data integrity and regulatory adherence across QC processes, acting as a liaison between QC and QA Operations and engaging with senior site stakeholders.

As a Quality and Compliance representative, you will drive CAPA, investigations and SOP revisions while partnering with cross-functional teams to uphold quality standards and support regulatory inspections.

Qualifikationen

• Academic degree in Chemistry/Biochemistry/Biotechnology/Life Science or related field.
• Profound working experience in the pharmaceutical industry within QC/QA.
• Analytical expertise with method validation, change management and deviation handling.
• Strong background in cGMPs, USP/EP regulations; audits with Health Authorities.
• Experience in cross-functional teamwork and regulatory inspections.

Aufgaben

• Represent QA Analytics in cross-functional teams and meetings.
• Ensure GxP requirements and SOPs are followed across QC and QA operations.
• Review and approve QC/AD documents, method transfer and validation files.
• Drive CAPA items and investigations to completion and timely closure.
• Provide SME guidance for QA Analytics and support regulatory inspections.

Kenntnisse

Cross-functional teamwork

Excellent English communication

Ausbildung

Chemistry/Biochemistry/Biotechnology/Life Science

Jobbeschreibung

Lonza is seeking a QA Manager (f/m/d) within QA Analytics in Visp, Switzerland. You will ensure GxP compliance, data integrity and regulatory adherence across QC processes, acting as a liaison between QC and QA Operations and engaging with senior site stakeholders.

As a Quality and Compliance representative, you will drive CAPA, investigations and SOP revisions while partnering with cross-functional teams to uphold quality standards and support regulatory inspections.