The actual location of this job is in Stein, AG, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed. The role is primarily site‑based; however, remote work is allowed for no more than 20% of the time, subject to case‑by‑case business needs. Benefits
An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Competitive salary plus numerous lifestyle, family, and leisure benefits. Full list of global benefits available at https://www.lonza.com/careers/benefits. Responsibilities
Lead and coordinate QC related project activities for release and stability testing of late‑phase (PPQ) and commercial drug products, with a focus on large molecules and Antibody Drug Conjugates (ADCs). Serve as primary QC representative and project champion, driving project execution through effective coordination of timelines, deliverables, customer engagements, and stakeholder communication in close partnership with Program Managers. Assess laboratory capacity and manage analytical method transfers, ensuring timely implementation of testing to meet customer and project requirements. Implement analytical testing strategies, including method suitability assessments, performance evaluation, control strategies, and specification setting. Author quality records and cGMP documents (e.g., procedures, source documents, reports, deviations, change requests). Act as QC subject matter expert during audits, inspections, and customer meetings while ensuring GMP‑compliant documentation and regulatory readiness. Qualifications
Work experience in a GMP‑regulated pharmaceutical QC environment with a sound understanding of analytical testing of biologics (large molecules) is required. Strong collaboration and stakeholder management skills, with confidence to coordinate activities, provide constructive challenge, and interact effectively with customers and internal teams. Experience in project coordination, analytical method validation and/or method transfer is a strong advantage. Fluency in English is required; fluency in German is a plus. Degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related life sciences discipline.
#J-18808-Ljbffr
An agile career and a dynamic work culture. An inclusive and ethical workplace. Compensation programs that recognize high performance. Competitive salary plus numerous lifestyle, family, and leisure benefits. Full list of global benefits available at https://www.lonza.com/careers/benefits. Responsibilities
Lead and coordinate QC related project activities for release and stability testing of late‑phase (PPQ) and commercial drug products, with a focus on large molecules and Antibody Drug Conjugates (ADCs). Serve as primary QC representative and project champion, driving project execution through effective coordination of timelines, deliverables, customer engagements, and stakeholder communication in close partnership with Program Managers. Assess laboratory capacity and manage analytical method transfers, ensuring timely implementation of testing to meet customer and project requirements. Implement analytical testing strategies, including method suitability assessments, performance evaluation, control strategies, and specification setting. Author quality records and cGMP documents (e.g., procedures, source documents, reports, deviations, change requests). Act as QC subject matter expert during audits, inspections, and customer meetings while ensuring GMP‑compliant documentation and regulatory readiness. Qualifications
Work experience in a GMP‑regulated pharmaceutical QC environment with a sound understanding of analytical testing of biologics (large molecules) is required. Strong collaboration and stakeholder management skills, with confidence to coordinate activities, provide constructive challenge, and interact effectively with customers and internal teams. Experience in project coordination, analytical method validation and/or method transfer is a strong advantage. Fluency in English is required; fluency in German is a plus. Degree in Chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related life sciences discipline.
#J-18808-Ljbffr
Project Lead QC 80-100% Arbeitgeber: Lonza Group Ltd.
Die Lonza Group Ltd. ist ein hervorragender Arbeitgeber, der seinen Mitarbeitenden in der Region Oberwallis nicht nur ein wettbewerbsfähiges Gehalt, sondern auch ein unterstützendes und innovatives Arbeitsumfeld bietet. Unsere Unternehmenskultur fördert die persönliche und berufliche Weiterentwicklung, während wir gleichzeitig großen Wert auf Sicherheit und Teamarbeit legen. Als Werkstattleiter haben Sie die Möglichkeit, Prozesse zu optimieren und Ihr Team aktiv zu führen, was Ihnen eine bedeutende Rolle in unserem Unternehmen verleiht.
