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QC Analyst II(m/w/x)
Evaluating lab results and managing GxP documentation in a pharmaceutical laboratory for patient-focused biotech. GMP experience and proficiency in analytical technologies required. Shift work for continuous laboratory operations.
Requirements
- Experience in quality assurance and analytical skills
- Proficiency in analytical technologies
- Knowledge of lab-specific software
- GMP experience and technological expertise
- Willingness to work in shifts
- Fluency in German and English
- Collaboration and communication skills
- Data integrity and deadline adherence
- Ability to deal with ambiguity
- Digital saviness
- Knowledge of health and safety regulations
- Leadership and monitoring skills
- Problem solving skills and punctuality
- Knowledge of regulatory requirements
Tasks
- Maintain compliance with current Standard Operating Procedures
- Manage GxP-compliant documentation and records
- Perform analytical tasks in a pharmaceutical laboratory
- Evaluate laboratory results and data
- Work flexible shifts as required by laboratory operations
- Ensure the integrity of quality assurance records
- Foster collaboration between the team and other departments
- Maintain a high level of GxP knowledge and education
- Support quality audits and health authority inspections
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- HPLC
- GC
- titration
- Empower
- Chromeleon
- TiAmo
Benefits
Informal Culture
- Inclusive work environment
Other Benefits
- Reasonable accommodation
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QC Analyst II(m/w/x)
Evaluating lab results and managing GxP documentation in a pharmaceutical laboratory for patient-focused biotech. GMP experience and proficiency in analytical technologies required. Shift work for continuous laboratory operations.
Requirements
- Experience in quality assurance and analytical skills
- Proficiency in analytical technologies
- Knowledge of lab-specific software
- GMP experience and technological expertise
- Willingness to work in shifts
- Fluency in German and English
- Collaboration and communication skills
- Data integrity and deadline adherence
- Ability to deal with ambiguity
- Digital saviness
- Knowledge of health and safety regulations
- Leadership and monitoring skills
- Problem solving skills and punctuality
- Knowledge of regulatory requirements
Tasks
- Maintain compliance with current Standard Operating Procedures
- Manage GxP-compliant documentation and records
- Perform analytical tasks in a pharmaceutical laboratory
- Evaluate laboratory results and data
- Work flexible shifts as required by laboratory operations
- Ensure the integrity of quality assurance records
- Foster collaboration between the team and other departments
- Maintain a high level of GxP knowledge and education
- Support quality audits and health authority inspections
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- HPLC
- GC
- titration
- Empower
- Chromeleon
- TiAmo
Benefits
Informal Culture
- Inclusive work environment
Other Benefits
- Reasonable accommodation
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Pharma Schweizerhalle AG
Industry
Pharmaceuticals
Description
The company is committed to helping people with disease and their families through innovative science and a supportive community.
Not a perfect match?
- Novartis Pharma Schweizerhalle AG
QC Analyst II(m/w/x)
Full-timeOn-siteExperiencedBasel - 1201 F. Hoffmann-La Roche AG
Laborant in der Analytik–QC PAT(m/w/x)
Full-timeTemporary contractOn-siteExperiencedKaiseraugst - 1201 F. Hoffmann-La Roche AG
QC Laboratory Technician in der Unit Large Molecule HPLC(m/w/x)
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Laboratory Scientist Phys-Chemical QC(m/w/x)
Full-timeOn-siteExperiencedBasel - Lonza
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