Skills this job asks for
AgileComplianceSAPGermanEnglishCommunicationRecruitment
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Sponsorship verdict
No sponsorship evidence yet
No government record and no wording either way. Not a refusal: ask the recruiter.
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No government sponsor record hereThis employer posted directly and does not match a government sponsor register.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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Can’t check pay against the visa rulesWe don’t have visa salary rules for this country yet.
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Before you apply
Sponsorship unknown
No register record and no sponsorship wording in the posting. Worth asking the employer before investing significant time.
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About the role
**Administrator (40% flexible)**Join our Quality Control team in Visp to coordinate essential workflows, manage GMP documentation, and support seamless team operations in a flexible part\-time role.This is a 40% fully site\-based role. Working together in person supports close, real\-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards.**What you will get:*** An agile career and dynamic working culture.* An inclusive and ethical workplace.**What you will do:*** Coordinate and organize end\-to\-end training activities across the Quality Control (QC) organization to ensure team readiness and compliance.* Maintain, track, and update training records and GMP\-relevant documentation within internal quality systems.* Support critical documentation workflows, including the physical archiving and indexing of laboratory raw data.* Assist with the administrative onboarding process for new team members to ensure a smooth transition into the QC environment.* Maintain, verify, and update operational data and records in SAP and relevant Lonza databases.* Identify opportunities to streamline and optimize administrative and training coordination processes within the team.* Provide general organizational and administrative support to the broader QC team on daily operational priorities.**What we are looking for:*** **Fluent command of both German and English (oral and written) is essential for this role*** Completed commercial apprenticeship (Kaufmännische Ausbildung), a scientific background with an aptitude for administration, or equivalent practical experience.* Prior experience working in a regulated environment (pharmaceutical, GMP, MedTech, or similar industry) is an advantage.* Demonstrated proficiency in MS Office applications; practical experience with SAP software is a strong plus.* Excellent organizational talents with a structured, precise, and highly reliable approach to managing administrative tasks.* Strong multi\-tasking skills with the ability to manage competing priorities independently.* Great team player with strong communication skills across diverse cross\-functional teams.**About Lonza** At Lonza, their people are their greatest strength. With 30\+ sites across five continents, their globally connected teams work together every day to manufacture the medicines of tomorrow. Their core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who they are and how they work together.Everyone’s ideas, big or small, have the potential to improve millions of lives, and that’s the kind of work they want you to be part of. Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, they value diversity and are committed to creating an inclusive environment.As Lonza’s talent acquisition partner, please note, Randstad is responsible for the engagement and contracting of this contingent role. Ready to play your part in shaping the future of life sciences? Apply now.j4id10447648jm j4it1043jm j4iy26jm
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