Process Engineer m/f/d

Aristo Group; Luzern; Vor Ort; CHF 90.000 - 130.000; Vollzeit

Zusammenfassung

Aristo Group in Lucerne, Switzerland, invites applications for a Process Engineer (m/f/d) in Upstream Operations. The role requires full onsite presence to integrate with an established team and support GMP manufacturing of early-phase clinical therapies.

The position emphasizes setting up and troubleshooting upstream processes, adherence to GMP and EHS standards, and involvement in continuous improvement with new technologies.

Qualifikationen

• Educational background in a relevant discipline.
• Minimum 3 years of work experience in the pharmaceutical or biotech industry.
• Ability to solve problems and learn quickly in a GMP environment.

Aufgaben

• Set up, execute, and troubleshoot upstream processes under GMP.
• Ensure GMP/EHS compliance in area of responsibility.
• Contribute to continuous improvement and evaluate new technologies.
• Create or update SOPs and master batch records; perform technical reviews.
• Participate in sampling activities and on-call duties as needed.

Kenntnisse

upstream

bioprocess

german

Ausbildung

Educational background in a relevant discipline

Jobbeschreibung

This is an Associate Specialist position within the Upstream Operations group at our company in the greater Lucerne area. This position requires full-time physical presence at the site to support manufacturing and to enable optimal integration into an existing team.

As a member of the manufacturing team at our company, you will be responsible for supporting various activities related to the implementation and GMP manufacturing of early-phase clinical therapies.

Project title: Process Engineer m/f/d

Type of employment: Payroll

Skills: upstream,bioprocess ,german

Project start: ASAP

Location: Lucerne, Switzerland - fully onsite

Tasks:

• Set up, practical execution and troubleshooting of upstream processes under GoodManufacturing Practices (GMP)
• Knowledge of and compliance to GMP principles and EHS standards in the area ofresponsibility
• Involvement in continuous improvement efforts and support for the implementation ofnew technologies, including non-GMP engineering runs or testing activities
• Creation and updates of SOPs and (electronic) master batch records. Technical review ofvarious documentation related to process transfer and GMP manufacturing
• Participation in sampling activities (including occasional weekend work) or on-callduties, as required by the process scheduling. Typical manufacturing activities do notinclude shift work

Qualifications:

• Educational background in a relevant discipline
• A minimum of 3 years of work experience in the pharmaceutical or biotech industry.
• Ability to solve problems and take new perspectives on existing solutions with a desire to continuously learn, improve and developAbility to perform under pressure in a complex GMP environment and assume responsibility.
• Flexible attitude when working with internal or external stakeholders to achieve ambitious targets.
• Business Fluent in English and German:Effective oral / written communication skills in German (C1)Oral / written communication skills in English (B2+)
• Residence within approximately 30 minutes commuting distance from Schachen (LU) or willingness to relocate
• Driver’s license (B) and access to a personal car to enable on-call duties