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Process Engineer m/w/d (DE)

[16604]
Process engineering, GMP

This full-time, on-site role within the Process Operations team in the greater Lucerne area focuses on upstream manufacturing activities for early-phase clinical therapies. The position supports GMP operations and continuous improvement initiatives in a dynamic biotech environment. Project title: Process Engineer m/w/d Type of employment: Payroll Industry: Biotech Skills: Process engineering,GMP Project start: 01.10.2025 Project duration: 12 months Location: Lucerne, Switzerland Tasks: ·Execute and troubleshoot upstream operations in continuous and fed-batch processes under GMP ·Ensure compliance with GMP and EHS standards ·Support non-GMP engineering runs and implementation of new technologies ·Create and revise SOPs and electronic master batch records; review technical documentation ·Manage materials using ERP systems (SAP) ·Participate in sampling activities and occasional on-call duties (no shift work required) Qualifications: ·Educational background in a relevant scientific discipline ·0–2 years of experience in pharmaceutical or biotech industry ·Strong problem-solving skills and a proactive, learning-oriented mindset ·Ability to perform under pressure and collaborate with internal/external stakeholders ·Fluent in German (C1) and proficient in English (B2+) ·Residence within ~30 minutes of Schachen (LU) or willingness to relocate ·Valid driver’s license (B) and access to a personal vehicle

This full-time, on-site role within the Process Operations team in the greater Lucerne area focuses on upstream manufacturing activities for early-phase clinical therapies. The position supports GMP operations and continuous improvement initiatives in a dynamic biotech environment.

Project title: Process Engineer m/w/d
Type of employment: Payroll
Industry: Biotech
Skills: Process engineering,GMP
Project start: 01.10.2025
Project duration: 12 months
Location: Lucerne, Switzerland

Tasks:
  • Execute and troubleshoot upstream operations in continuous and fed-batch processes under GMP
  • Ensure compliance with GMP and EHS standards
  • Support non-GMP engineering runs and implementation of new technologies
  • Create and revise SOPs and electronic master batch records; review technical documentation
  • Manage materials using ERP systems (SAP)
  • Participate in sampling activities and occasional on-call duties (no shift work required)
Qualifications:
  • Educational background in a relevant scientific discipline
  • 0–2 years of experience in pharmaceutical or biotech industry
  • Strong problem-solving skills and a proactive, learning-oriented mindset
  • Ability to perform under pressure and collaborate with internal/external stakeholders
  • Fluent in German (C1) and proficient in English (B2+)
  • Residence within ~30 minutes of Schachen (LU) or willingness to relocate
  • Valid driver’s license (B) and access to a personal vehicle





map Lucerne, Switzerland date_range 01.10.2025 update Temporary
Direkter Kontakt

Tünde Verebélyi

Senior Consultant
mail t.verebelyi@aristo-group.com
phone +41 44 274 39 00


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