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Master data management and harmonization in SingleLIMS, ASPIRE, Speca for pharmaceutical lab systems at a healthcare science company. 3+ years pharmaceutical industry experience and quality assurance background required; LPS methodology familiarity preferred. Work with global data interfaces and multi-site teams.
Requirements
- Degree in life sciences
- 3+ years pharmaceutical industry experience
- Experience in quality assurance or testing
- Preferably experience in pharmaceutical IT systems
- Familiarity with LPS methodology
- Extensive expertise in cGMP
- Knowledge of local and international GMP
- Independent handling of challenging tasks
- Analytical ability and decision-making skills
- Professional and results-oriented work style
- Focus on continuous improvement
- Integrative personality and communication skills
- Ability to build trusting relationships
- Fluent German or English communication skills
Tasks
- Manage local master data within SingleLIMS, ASPIRE, and Speca
- Provide operational support for systems including incident management
- Handle system documentation and reporting
- Harmonize local master data across Basel, Kaiseraugst, and global interfaces
- Drive continuous improvements in local lab systems
- Facilitate information flow within and outside the organizational area
- Develop and execute QC strategies with local and global partners
- Represent the department during audits and inspections
- Ensure procedures and documentation remain regulatory compliant and inspection-ready
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LPS methodology
- cGMP
- GMP regulations
- IT systems
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Master data management and harmonization in SingleLIMS, ASPIRE, Speca for pharmaceutical lab systems at a healthcare science company. 3+ years pharmaceutical industry experience and quality assurance background required; LPS methodology familiarity preferred. Work with global data interfaces and multi-site teams.
Requirements
- Degree in life sciences
- 3+ years pharmaceutical industry experience
- Experience in quality assurance or testing
- Preferably experience in pharmaceutical IT systems
- Familiarity with LPS methodology
- Extensive expertise in cGMP
- Knowledge of local and international GMP
- Independent handling of challenging tasks
- Analytical ability and decision-making skills
- Professional and results-oriented work style
- Focus on continuous improvement
- Integrative personality and communication skills
- Ability to build trusting relationships
- Fluent German or English communication skills
Tasks
- Manage local master data within SingleLIMS, ASPIRE, and Speca
- Provide operational support for systems including incident management
- Handle system documentation and reporting
- Harmonize local master data across Basel, Kaiseraugst, and global interfaces
- Drive continuous improvements in local lab systems
- Facilitate information flow within and outside the organizational area
- Develop and execute QC strategies with local and global partners
- Represent the department during audits and inspections
- Ensure procedures and documentation remain regulatory compliant and inspection-ready
Work Experience
- 3 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- LPS methodology
- cGMP
- GMP regulations
- IT systems
About the Company
Roche
Industry
Healthcare
Description
The company is dedicated to advancing science and ensuring access to healthcare for everyone.
Not a perfect match?
- Novartis Pharma Schweizerhalle AG
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