PIERRE FABRE PHARMA AG
Laborantin(e) en chimie(m/w/x)
Full-timeOn-siteJunior
Palézieux
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SUSUSONITY
Associate Scientist(m/w/x)
Corsier-sur-Vevey
Full-timeOn-siteExperienced
Nejo AI Summary
Routine analytical testing and method qualification for oncology and neurology medicines. ≥5 years in GMP analytical lab required. Diverse, inclusive, and flexible working culture.
Requirements
- CFC or Master in Chemistry, Pharmacy, Biology, or Biotechnology
- ≥5 years in GMP analytical lab
- Proficient with (L)LIMS
- Empower and/or Waters Connect a plus
- Comfortable writing GMP analytical protocols, reports, and SOPs
- Strong knowledge of Liquid Chromatography and/or Mass Spectrometry
- Routine testing, troubleshooting, cleaning of LC/MS
- Knowledge of CMC NBE/ADC development
- ADC knowledge is a strong asset
- Familiar with GMP/Quality Systems
- Familiar with international guidelines (ICH, Pharmacopeias)
- Capable of performing routine and non-routine analyses
- Able to sort deviations, CAPA, and lead investigations for QC
- Team player
- Solid English skills
- French skills a plus
- Curious about new tools/tech
- Proactive in proposing solutions and driving improvements
- On-call duties
- 6S experience
- Strong planning skills
- 4-9 years professional experience
Tasks
- Conduct routine analytical testing and method qualification
- Perform stability testing in Liquid Chromatography and Capillary Electrophoresis
- Execute MS-based method qualification
- Deliver high-quality data treatment and analytical reports
- Interact with customers to discuss results and coordinate activities
- Work independently on routine and non-routine tasks
- Apply specialized technical knowledge in stability testing
- Demonstrate strong expertise in a GMP environment
- Validate GMP methods and documentation
- Lead analytical workflow improvement initiatives
- Present and defend topics during health authority inspections
- Write GMP documentation including URS, protocols, reports, SOPs, deviations, CAPA, and CCP actions
Work Experience
- 4 - 9 years
Education
- Vocational certification
Languages
- English – Native
- French – Basic
Tools & Technologies
- (L)LIMS
- Empower
- Waters Connect
- Liquid Chromatography
- Mass Spectrometry
- ICH
- Pharmacopeias
Benefits
Informal Culture
- Diverse, inclusive and flexible working culture
Learning & Development
- Personal development opportunities
Career Advancement
- Career advancement opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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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SUSUSONITY
Associate Scientist(m/w/x)
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Full-timeOn-siteExperienced
Nejo AI Summary
Routine analytical testing and method qualification for oncology and neurology medicines. ≥5 years in GMP analytical lab required. Diverse, inclusive, and flexible working culture.
Requirements
- CFC or Master in Chemistry, Pharmacy, Biology, or Biotechnology
- ≥5 years in GMP analytical lab
- Proficient with (L)LIMS
- Empower and/or Waters Connect a plus
- Comfortable writing GMP analytical protocols, reports, and SOPs
- Strong knowledge of Liquid Chromatography and/or Mass Spectrometry
- Routine testing, troubleshooting, cleaning of LC/MS
- Knowledge of CMC NBE/ADC development
- ADC knowledge is a strong asset
- Familiar with GMP/Quality Systems
- Familiar with international guidelines (ICH, Pharmacopeias)
- Capable of performing routine and non-routine analyses
- Able to sort deviations, CAPA, and lead investigations for QC
- Team player
- Solid English skills
- French skills a plus
- Curious about new tools/tech
- Proactive in proposing solutions and driving improvements
- On-call duties
- 6S experience
- Strong planning skills
- 4-9 years professional experience
Tasks
- Conduct routine analytical testing and method qualification
- Perform stability testing in Liquid Chromatography and Capillary Electrophoresis
- Execute MS-based method qualification
- Deliver high-quality data treatment and analytical reports
- Interact with customers to discuss results and coordinate activities
- Work independently on routine and non-routine tasks
- Apply specialized technical knowledge in stability testing
- Demonstrate strong expertise in a GMP environment
- Validate GMP methods and documentation
- Lead analytical workflow improvement initiatives
- Present and defend topics during health authority inspections
- Write GMP documentation including URS, protocols, reports, SOPs, deviations, CAPA, and CCP actions
Work Experience
- 4 - 9 years
Education
- Vocational certification
Languages
- English – Native
- French – Basic
Tools & Technologies
- (L)LIMS
- Empower
- Waters Connect
- Liquid Chromatography
- Mass Spectrometry
- ICH
- Pharmacopeias
Benefits
Informal Culture
- Diverse, inclusive and flexible working culture
Learning & Development
- Personal development opportunities
Career Advancement
- Career advancement opportunities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of SUSONITY 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.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
SUSONITY
Industry
Pharmaceuticals
Description
Das Unternehmen entwickelt Medikamente, intelligente Geräte und innovative Technologien in Therapiegebieten wie der Onkologie, Neurologie und Fruchtbarkeit.
Not a perfect match?
- PIERRE FABRE PHARMA AG
Laborantin(e) en chimie(m/w/x)
Full-timeOn-siteJuniorPalézieux - Ferring Pharmaceuticals
Analytical Development Intern(m/w/x)
Full-timeInternshipOn-siteÉpalinges - SUSONITY
Internship - Process Development of ADCs(m/w/x)
Full-timeInternshipOn-siteCorsier-sur-Vevey - Adaptyv
Head of QC & Analytics(m/w/x)
Full-timeOn-siteSeniorLausanne - SUSONITY
Internship: Automated At-line UPLC for GxP(m/w/x)
Full-timeInternshipOn-siteCorsier-sur-Vevey