F. Hoffmann-La Roche AG
Complaint Lead Investigator(m/w/x)
Full-timeOn-siteSenior
Kaiseraugst
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121201 F. Hoffmann-La Roche AG
QC Investigator(m/w/x)
Kaiseraugst
Full-timeOn-siteExperienced
Nejo AI Summary
Leading critical quality deviations and root cause analysis for pharmaceutical manufacturing at global pharma with 100,000+ employees. Extensive cGMP expertise and 3+ years pharma industry experience required. Exposure to global quality standards and regulations.
Requirements
- Degree in Life Sciences
- 3+ years of professional experience in pharmaceutical industry
- Experience in Quality Assurance or QC testing
- Extensive expertise in cGMP
- Knowledge of local and international GMP regulations
- Proficiency in LPS methodology
- Knowledge of root cause analysis
- Analytical ability to evaluate complex issues
- Results-oriented decision making
- Excellent communication skills in German or English
- Collaboration skills across global network
Tasks
- Lead critical and complex deviations and investigations
- Focus on quality KPIs to maintain high standards
- Support and guide deviation huddles for the QC organization
- Contribute to root cause analysis and implement CAPA measures
- Oversee improvement activities in deviations and investigations
- Enhance technical writing standards within the QC organization
- Collaborate with teams to ensure safety and reliability in analytical processes
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of 1201 F. Hoffmann-La Roche AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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121201 F. Hoffmann-La Roche AG
QC Investigator(m/w/x)
Kaiseraugst
Full-timeOn-siteExperienced
Nejo AI Summary
Leading critical quality deviations and root cause analysis for pharmaceutical manufacturing at global pharma with 100,000+ employees. Extensive cGMP expertise and 3+ years pharma industry experience required. Exposure to global quality standards and regulations.
Requirements
- Degree in Life Sciences
- 3+ years of professional experience in pharmaceutical industry
- Experience in Quality Assurance or QC testing
- Extensive expertise in cGMP
- Knowledge of local and international GMP regulations
- Proficiency in LPS methodology
- Knowledge of root cause analysis
- Analytical ability to evaluate complex issues
- Results-oriented decision making
- Excellent communication skills in German or English
- Collaboration skills across global network
Tasks
- Lead critical and complex deviations and investigations
- Focus on quality KPIs to maintain high standards
- Support and guide deviation huddles for the QC organization
- Contribute to root cause analysis and implement CAPA measures
- Oversee improvement activities in deviations and investigations
- Enhance technical writing standards within the QC organization
- Collaborate with teams to ensure safety and reliability in analytical processes
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of 1201 F. Hoffmann-La Roche AG and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
About the Company
1201 F. Hoffmann-La Roche AG
Industry
Pharmaceuticals
Description
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
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