The actual location of this job is in Visp, Switzerland. Relocation assistance is available for eligible candidates and their families, if needed.
What you will get: An agile career with opportunities for professional growth in a global life sciences organization
A collaborative, inclusive, and ethical workplace where diverse perspectives are valued
Competitive compensation and recognition programs that reward high performance
Access to a wide range of local and global benefits, depending on role and location
What you will do: Support piloting and production campaigns and ensure plant operation and technical support, including outside regular working hours as part of the on-call service.
Create, maintain and optimize cGMP-compliant documentation such as SOPs, HSPs and checklists in close collaboration with MSAT and operational biotechnologists
Ensure that technical and operational requirements are considered early in the planning and engineering phases of projects
Coordinate and support engineering, workshop and technical teams during investments, plant preparation activities and technical improvement initiatives
Monitor production activities, ensure adherence to planned work and initiate corrective actions in the event of deviations
Contribute to the technical instruction and training of employees and support teams with plant-related technical questions
Continuously improve equipment, processes and workflows according to Lean, Kaizen and 6S principles while complying with safety, quality, hygiene and environmental standards
What we are looking for: Completed vocational training as a chemical and pharmaceutical technologist, chemical or biological laboratory technician, or a university degree at bachelor's or master's level in biotechnology, pharmaceutical sciences or a related field
Several years of experience in a GMP-regulated production environment or in a comparable pharmaceutical or biotechnological function
Sound knowledge of process equipment and automation systems, in particular DeltaV/MES
Strong technical understanding and the ability to approach technical challenges in a structured and solution-oriented manner
Experience in creating and maintaining GMP-relevant documentation and working with cross-functional teams
Very good written and spoken German skills; English skills are desirable
Commitment to continuous improvement and a strong awareness of quality, safety, hygiene and environmental standards
About Lonza At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.
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Manufacturing Line Specialist - Anlagemeister 80-100% (w/m/d) Arbeitgeber: Lonza
Lonza ist ein hervorragender Arbeitgeber, der eine dynamische Arbeitskultur und flexible Arbeitsmöglichkeiten bietet, um die besten Talente zu fördern. Mit einem starken Fokus auf persönliche Entwicklung und Teamarbeit ermöglicht Lonza seinen Mitarbeitern, ihre Karriere in einem bedeutenden Bereich wie der internen Revision voranzutreiben, während sie gleichzeitig zur Verbesserung von Millionen von Leben beitragen. Die enge Zusammenarbeit vor Ort fördert nicht nur den Austausch von Ideen, sondern auch die technische Präzision, die für die Herstellung von Arzneimitteln erforderlich ist.
