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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Roche
Industry
Healthcare
Description
The company is dedicated to advancing science and ensuring access to healthcare for everyone.
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