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Master Data Manager for ASPIRE and SingleLIMS within Synthetic Molecules Technical Development - Lab Support & Compliance(m/w/x)
Description
In this role, you will manage analytical master data and establish workflows while collaborating with various teams. Your day-to-day responsibilities will include authoring SOPs, providing user support, and ensuring effective communication across departments.
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Requirements
- •Graduation in a scientific field or equivalent skills
- •Strong affinity and interest in Systems, Databases, and GMP Compliance
- •Autonomy, reliability, attention to detail, and teamwork skills
- •Digital skills and high affinity for databases
- •Experience in the pharmaceutical industry and strong GMP understanding
- •Flexibility, prioritization, and reliability under pressure
- •Autonomy and continuous learning
- •High ability for relationship-building and coordination skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Set up GMP and non-GMP analytical master data in SingleLIMS and ASPIRE
- •Establish connections between existing and future systems and interfaces
- •Collaborate with PTD teams to create new workflows and processes
- •Author and update SOPs and working procedures
- •Provide user training and support on ASPIRE and SingleLIMS
- •Manage troubleshooting and system adaptations
- •Collaborate with global functions and other departments
- •Ensure regular communication and networking with other sites
- •Facilitate continuous improvement and harmonization
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
- 1201 F. Hoffmann-La Roche AGFull-timeTemporary contractOn-siteExperiencedBasel
- Roche
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Master Data Manager for ASPIRE and SingleLIMS within Synthetic Molecules Technical Development - Lab Support & Compliance(m/w/x)
The AI Job Search Engine
Description
In this role, you will manage analytical master data and establish workflows while collaborating with various teams. Your day-to-day responsibilities will include authoring SOPs, providing user support, and ensuring effective communication across departments.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Graduation in a scientific field or equivalent skills
- •Strong affinity and interest in Systems, Databases, and GMP Compliance
- •Autonomy, reliability, attention to detail, and teamwork skills
- •Digital skills and high affinity for databases
- •Experience in the pharmaceutical industry and strong GMP understanding
- •Flexibility, prioritization, and reliability under pressure
- •Autonomy and continuous learning
- •High ability for relationship-building and coordination skills
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Set up GMP and non-GMP analytical master data in SingleLIMS and ASPIRE
- •Establish connections between existing and future systems and interfaces
- •Collaborate with PTD teams to create new workflows and processes
- •Author and update SOPs and working procedures
- •Provide user training and support on ASPIRE and SingleLIMS
- •Manage troubleshooting and system adaptations
- •Collaborate with global functions and other departments
- •Ensure regular communication and networking with other sites
- •Facilitate continuous improvement and harmonization
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
About the Company
1201 F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
The company focuses on developing innovative products that make a meaningful difference for patients worldwide.
- 1201 F. Hoffmann-La Roche AG
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