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Process Engineer m/f/d
Job in
6000, Luzern, Kanton Luzern, Switzerland
Listed on 2026-09-12
Listing for:
Aristo Group
Full Time, Per diem
position Listed on 2026-09-12
Job specializations:
-
Manufacturing / Production
Validation Engineer, Pharmaceutical Manufacturing, Manufacturing Engineer, Quality Engineering -
Engineering
Validation Engineer, Manufacturing Engineer, Quality Engineering
Job Description & How to Apply Below
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 Good Manufacturing Practices (GMP)
- Knowledge of and compliance to GMP principles and EHS standards in the area of responsibility
- 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-call duties, as required by the process scheduling. Typical manufacturing activities do not include 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 develop
Ability 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
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