Junior Specialist Arbeitsvorbereitung (m/f/d) 80-100% — Lonza

Full description

The location of this location is in Stein, AG, Switzerland. Eligible applicants and their families will be assisted in moving if needed.

They support pharmaceutical manufacturing by carefully maintaining production data in the MES system, producing production documentation and preparing relevant production documents and labels. If you like to work accurately and structured, have a high level of quality awareness and take on responsibility in a closely collaborating team, you can expect a central function with great influence on a smooth production process. Your Career in Drug Product Services at Lonza

This body requires full presence on the ground. Personal collaboration enables close, timely collaboration and the technical precision required to produce pharmaceuticals to the highest quality and safety standards.

What awaits you

● An agile career and a dynamic work culture. ● An inclusive and ethical working environment ● Remuneration programs that recognize high performance. In addition to a competitive salary, you can expect numerous benefits for lifestyle, family and leisure. Our global benefits: https://www.lonza.com/careers/benefits Our local benefits: 3cf206339e0e4e41a77e8c806138c2b5

Their tasks

• They take over the work preparation and follow-up of production orders in the MES system as well as the preparation and maintenance of the associated GMP documentation and paper documents.
• They transfer production-relevant parameters from manufacturing specifications to Master Batch Records (MBRs) and ensure that all data, materials and documents are assigned to the correct batch.
• They produce sample labels and production documents with the utmost care and thus make an important contribution to a smooth and error-free production process.
• You ensure material availability in the MES system, work GMP-compliant and document your activities in a timely and comprehensible manner in accordance with the applicable requirements.
• They work closely with production, quality and other interfaces, support deviations and cause analyses and ensure that production employees can start production in an optimally prepared manner.

What we are looking for

• They have fluent knowledge of German, have basic knowledge of English and are confident in dealing with common PC applications such as Word and Excel.
• They work extremely precisely, concentrated and carefully and keep track of a large number of figures, data and documents, as well as under time pressure.
• You are characterized by an independent, structured working method and take responsibility for the quality of your results.
• You are a team-oriented personality, communicate openly and appreciate the close cooperation in a collegial environment.
• Ideally, you will have experience in the GMP-regulated environment as well as knowledge of SAP and/or MES systems.

About Lonza At Lonza, our employees are our greatest strength. At more than 30 locations on five continents, our globally networked teams work together every day to produce the medicines of tomorrow. Our core values: 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 exactly what we want you to share. Innovation thrives when people from different backgrounds bring in their unique perspectives. At Lonza, we value diversity and are committed to an inclusive environment for all employees. If you are ready to translate our customers’ groundbreaking ideas into viable therapies, we look forward to welcoming you on board. Ready to shape the future of life sciences? Apply now

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