Overview
Experience with a leading global Pharma/Biotech company and a 1-year temporary contract with strong potential for extension.
Our client, an internationally renowned pharmaceutical company, is currently looking for an Automation Engineer available from 1 October for the Lucerne area, to join an international team for a period of 12 months. Depending on the selected candidate's performance and motivation, there is a possibility of an extension or a permanent take over.
Responsibilities
* Execution, setup, and troubleshooting of upstream processes and support unit operations in both continuous manufacturing and fed-batch settings, conducted under Good Manufacturing Practice (GMP) standards
* 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
Qualifications
* 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)
What's on Offer
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!
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