[ref. d13342017] Process Engineer - Luzern

• Adherence to GMP principles and EHS regulations within the assigned scope of responsibility
• Contribution to ongoing process improvements and support in introducing new technologies, including non-GMP engineering runs or test activities
• Preparation and revision of SOPs and electronic master batch records, along with technical review of documentation related to process transfers and GMP production
• Management of materials through ERP systems (e.g., SAP)
• Engagement in sampling tasks (with occasional weekend work) or on-call duties as required by production schedules; standard manufacturing activities are not performed in shifts

• Academic background with a bachelor's or master's degree in a relevant discipline
• 0-2 years of professional experience in the pharmaceutical or biotechnology industry
• Strong problem-solving skills with the ability to approach existing challenges from new perspectives, combined with a drive for continuous learning, improvement, and personal development
• Capability to perform effectively under pressure in a complex GMP environment, taking ownership and responsibility. Flexible and collaborative mindset when working with both internal and external stakeholders to achieve ambitious objectives
• Business fluency in English and German: German: (C1 level) English: (B2+ level)
• Residence within approximately 30 minutes of Schachen (LU) or willingness to relocate
• Valid driver's license (B) with access to a personal vehicle to support on-call duties
• Prior hands-on experience in GMP biologics manufacturing, ideally including operation of bioreactors
• Familiarity with automated manufacturing systems (e.g., DeltaV) and electronic batch records (e.g., PAS-X)

Our client, an internationally renowned pharmaceutical company is currently looking for a Automation Engineer available from the 1. October for Lucerne area, to join an international team for a period of 12 months.

Depending on the selected candidate's performance and motivation, the possibility of an extension or a permanent take over.

Become part of a leading biopharmaceutical organization and play a key role in advancing upstream manufacturing under GMP standards. Take responsibility for cutting-edge processes, support the integration of new technologies, and contribute to the production of life-saving biologics in a highly dynamic environment.

Are you ready to take the next step in your career? We look forward to your application!