Aseptic Process Expert – Greenfield Growth (Stein)

Lonza

Stein

Vor Ort

Vertraulich

Vollzeit

Vor 6 Tagen
Sei unter den ersten Bewerbenden
Bewerbungsgenerator

Eine komplette Bewerbung in einer Minute — maßgeschneiderter Lebenslauf und Anschreiben, versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Dynamic work culture
Inclusive workplace
Competitive salary

Zusammenfassung

Lonza in Stein, AG, Switzerland, is seeking a highly motivated science professional to own aseptic compounding processes. You will lead GMP-compliant operations, support operators with technical expertise, and drive deviations, investigations and corrective actions to protect product quality.

This fully site-based role offers exposure to validation and qualification activities, inspection readiness, and collaboration with a proactive team.

Qualifikationen

  • Bachelor’s or Master’s degree in Life Sciences with hands-on aseptic/sterile manufacturing experience.
  • Experience in GMP-regulated manufacturing and quality/documentation requirements.
  • Fluent English and conversational German (B1 or higher) for cross‑functional communication.

Aufgaben

  • Lead and continuously improve aseptic compounding processes with GMP standards.
  • Provide hands-on technical support to operators and drive deviations/investigations.
  • Execute and support validation and qualification activities and maintain GMP documentation.
  • Keep equipment and processes inspection-ready and support audits.
  • Collaborate with a proactive team; strong ownership and flexibility in a fast-paced setting.

Kenntnisse

GMP manufacturing
Aseptic processing
Troubleshooting
Documentation
Validation
Teamwork
English fluent
German basic
Equipment maintenance

Ausbildung

Bachelor/Master in Life Sciences

Tools

GMP washers
Autoclaves
Sterilization equipment

Jobbeschreibung

Lonza in Stein, AG, Switzerland, is seeking a highly motivated science professional to own aseptic compounding processes. You will lead GMP-compliant operations, support operators with technical expertise, and drive deviations, investigations and corrective actions to protect product quality.

This fully site-based role offers exposure to validation and qualification activities, inspection readiness, and collaboration with a proactive team.

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