Process Expert, Drug Product 80-100%

Lonza

Stein

Vor Ort

Vertraulich

Vollzeit

14 Tage+

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Benefits dieser Stelle

Dynamic culture
Inclusive workplace
Performance rewards

Zusammenfassung

Lonza in Stein, Switzerland, is seeking a Process Expert to lead technical troubleshooting on an aseptic filling and lyophilization line. You will drive process improvements, train operators, manage deviations, and shape a new line from PQ through Swissmedic approval with significant autonomy.

You will collaborate with MSAT, QA and Engineering, ensuring cleanroom discipline and compliance across the line during a dynamic project phase. English proficiency is required; German is a plus.

Qualifikationen

  • Degree or equivalent in Life Science or Engineering.
  • Proven experience in aseptic filling or aseptic manufacturing in GMP environment.
  • Experience with lyophilization is highly preferred; Proficiency in English is a must.

Aufgaben

  • Ensure the production line runs efficiently and effectively.
  • Coordinate and support qualification of the manufacturing line to meet standards.
  • Identify weaknesses and determine solutions to fix or investigate issues.
  • Establish, drive and maintain cleanroom management practices.
  • Collaborate with MSAT, QA, Engineering to implement improvements and new processes.

Kenntnisse

Aseptic filling experience
GMP experience
Process troubleshooting
Cross-functional collaboration
English proficiency

Ausbildung

Degree in Life Science or Engineering

Jobbeschreibung

Location: Stein, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.

Join our antibody drug conjugate (ADC) manufacturing team as a Process Expert, where you will lead technical troubleshooting on an aseptic filling and lyophilization line, drive process improvements, train operators on the line, manage deviations and technical changes, and help shape the future of a state‑of‑the‑art production environment. This unique opportunity allows you to play a key role in ramping up a brand‑new line—from PQ and qualification through to Swissmedic approval—with significant autonomy, decision‑making responsibility, and the chance to define the processes that will set the standard for years to come.

What You Will Get
  • An agile career and a dynamic work culture.
  • An inclusive and ethical workplace.
  • Compensation programs that recognize high performance.

In addition to a competitive salary, you can expect numerous lifestyle, family, and leisure benefits. The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits

What You’ll Do
  • Act as the technical expert to ensure that the production line runs efficiently and effectively.
  • Coordinate and support the qualification of the manufacturing line, ensuring it meets strict industry standards.
  • Identify weaknesses in the production line and determine solutions to fix or investigate issues.
  • Establish, drive and maintain good cleanroom management practices.
  • Collaborate with team members and various internal functions (e.g., MSAT, QA, Engineering) to successfully implement improvements and new processes.
What We’re Looking For
  • Degree or equivalent experience in Life Science or Engineering.
  • Proven experience in either aseptic filling or aseptic manufacturing in a GMP‑controlled environment is a must; additional experience in qualification of manufacturing equipment is highly preferred.
  • Experience with lyophilization processes is highly preferred.Proficiency in English is a must; German is a plus.
  • Ability to move agilely between various tasks during this dynamic and exciting project phase. Demonstrates strong collaboration skills and actively supports team members.

Reference: R77950

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