Senior MSAT Equipment Qualification Leader

Lonza Group Ltd.; Stein; Sur place; EUR 197 000 - 262 000; Plein temps

Avantages offerts par ce poste

Agile career culture

Inclusive workplace

Competitive compensation

Résumé du poste

Lonza Group Ltd. is seeking a senior MSAT leader in Stein, Switzerland, to oversee Equipment Qualification and Process Platforms, ensuring lifecycle strategies, qualification governance, and deployment of single-use systems across sterile drug product manufacturing.

You will drive technical governance, collaborate with PHAD, MSAT Tech Transfer, Engineering, and Operations, and lead a high-performing team to deliver robust manufacturing processes in a regulated environment.

Qualifications

• MSc or PhD in Pharmaceutical Sciences, Pharmaceutical Engineering, Chemistry, Bioengineering, Biochemistry, or a related discipline.
• Sterile drug product manufacturing experience is a must.
• Experience with equipment qualification, lifecycle management, process validation, and aseptic technologies.
• Strong GMP and regulatory knowledge, with audit support experience.
• Excellent communication, stakeholder management, and leadership abilities; fluent in English; German is a plus.

Responsabilités

• Lead the Equipment Qualification & Process Platforms function, with accountability for people, resources, priorities and delivery.
• Develop MSAT expertise through resource planning, coaching, talent development and succession planning.
• Set strategic direction for Equipment Qualification and Process Platform activities, translating priorities into functional objectives.

Connaissances

Equipment qualification

Lifecycle management

Process validation

Aseptic manufacturing

GMP knowledge

Stakeholder management

Leadership

English fluency

Formation

MSc/PhD in Pharmaceutical Sciences or related

Description du poste

Lonza Group Ltd. is seeking a senior MSAT leader in Stein, Switzerland, to oversee Equipment Qualification and Process Platforms, ensuring lifecycle strategies, qualification governance, and deployment of single-use systems across sterile drug product manufacturing.

You will drive technical governance, collaborate with PHAD, MSAT Tech Transfer, Engineering, and Operations, and lead a high-performing team to deliver robust manufacturing processes in a regulated environment.