Sterile Fill & Finish Process Expert (GMP)

Lonza Group; Stein (AR); On-site; Vertraulich; Full time

Benefits offered by this job

Relocation assistance

Competitive salary

Lifestyle benefits

Job summary

Lonza in Stein (AG), Switzerland, seeks a Process Expert to support aseptic manufacturing on two sterile fill & finish lines. This site-based role emphasizes teamwork, precision, and adherence to GMP, quality, and safety standards.

Relocation assistance is available for eligible candidates and their families. You will collaborate with operators to ensure batches are produced on time, support validations and improvements, and lead investigations while maintaining strict cleanroom practices and

Qualifications

• Proven experience with aseptic manufacturing processes in a GMP environment.
• Experience with fill-finish processes of drug products (vials) desirable.
• Fluency in English and German required.
• Ability to move between multiple tasks in a dynamic environment.

Responsibilities

• Provide front line support to manufacturing, working with the operator to ensure batches are produced safely, on time and in compliance with instructions and quality requirements.
• Support the execution of process validations, re-validations and short-term improvement projects.
• Lead investigations and deviations and determine solutions to fix.
• Establish and maintain cleanroom management practices and audit readiness.
• Collaborate with cross-functional teams to implement improvements and new processes.

Skills

GMP experience

Aseptic manufacturing

English fluency

German fluency

Cross-functional collaboration

Education

Life Science or Engineering degree

Job description

Lonza in Stein (AG), Switzerland, seeks a Process Expert to support aseptic manufacturing on two sterile fill & finish lines. This site-based role emphasizes teamwork, precision, and adherence to GMP, quality, and safety standards.

Relocation assistance is available for eligible candidates and their families. You will collaborate with operators to ensure batches are produced on time, support validations and improvements, and lead investigations while maintaining strict cleanroom practices and