Dein persönlicher KI-Karriere-Agent
Associate Principal Scientist QC(m/w/x)
Leading advanced analytical activities and method development for pharmaceutical manufacturing. Extensive GMP QC experience with LC-MS and GC-MS expertise required. Relocation assistance, high-performance bonuses.
Anforderungen
- Master’s or PhD in chemistry, biochemistry, biotechnology, pharmacy, or related field
- Extensive experience in QC or analytical development in GMP environment
- Strong hands-on expertise in chromatography and mass spectrometry, particularly LC-MS and GC-MS
- Proven track record in analytical method development, validation, and optimization
- Solid knowledge of GMP regulations and global quality and compliance standards
- Strong technical and analytical problem-solving skills in instrumental analytics
- Demonstrated leadership abilities with capacity to guide, support, and develop team members
- Clear and confident communication skills in German and English
Aufgaben
- Lead advanced analytical activities
- Support quality control standards
- Take responsibility for defined QC sub-areas
- Ensure high analytical standards
- Plan and coordinate method development
- Develop LC-MS and GC-MS methods
- Validate and optimize analytical methods
- Execute routine analytical methods
- Provide technical expertise in instrumental analytics
- Act as an expert within the team
- Author and review SOPs
- Review testing procedures
- Review validation reports
- Investigate analytical issues
- Lead OOS and OOT assessments
- Train and mentor scientists
- Train laboratory colleagues
- Represent QC in cross-functional teams
- Represent QC during audits
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- LC-MS
- GC-MS
Benefits
Boni & Prämien
- Compensation programs for high performance
Mitarbeiterrabatte
- Wide range of lifestyle, family, and leisure benefits
- Access to locally tailored benefits
Sonstige Vorteile
- Relocation assistance
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Noch nicht perfekt?
- LonzaVollzeitnur vor OrtBerufserfahrenVisp
- CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
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Laborant/in Quality Control(m/w/x)
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Associate Process Chemist(m/w/x)
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Associate Principal Scientist QC(m/w/x)
Leading advanced analytical activities and method development for pharmaceutical manufacturing. Extensive GMP QC experience with LC-MS and GC-MS expertise required. Relocation assistance, high-performance bonuses.
Anforderungen
- Master’s or PhD in chemistry, biochemistry, biotechnology, pharmacy, or related field
- Extensive experience in QC or analytical development in GMP environment
- Strong hands-on expertise in chromatography and mass spectrometry, particularly LC-MS and GC-MS
- Proven track record in analytical method development, validation, and optimization
- Solid knowledge of GMP regulations and global quality and compliance standards
- Strong technical and analytical problem-solving skills in instrumental analytics
- Demonstrated leadership abilities with capacity to guide, support, and develop team members
- Clear and confident communication skills in German and English
Aufgaben
- Lead advanced analytical activities
- Support quality control standards
- Take responsibility for defined QC sub-areas
- Ensure high analytical standards
- Plan and coordinate method development
- Develop LC-MS and GC-MS methods
- Validate and optimize analytical methods
- Execute routine analytical methods
- Provide technical expertise in instrumental analytics
- Act as an expert within the team
- Author and review SOPs
- Review testing procedures
- Review validation reports
- Investigate analytical issues
- Lead OOS and OOT assessments
- Train and mentor scientists
- Train laboratory colleagues
- Represent QC in cross-functional teams
- Represent QC during audits
Berufserfahrung
- ca. 4 - 6 Jahre
Ausbildung
- Master-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Tools & Technologien
- LC-MS
- GC-MS
Benefits
Boni & Prämien
- Compensation programs for high performance
Mitarbeiterrabatte
- Wide range of lifestyle, family, and leisure benefits
- Access to locally tailored benefits
Sonstige Vorteile
- Relocation assistance
Karriere- und Weiterentwicklung
- Agile career
Lockere Unternehmenskultur
- Dynamic work culture
Sinnstiftende Arbeit
- Inclusive and ethical workplace
Über das Unternehmen
Lonza
Branche
Pharmaceuticals
Beschreibung
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
Noch nicht perfekt?
- Lonza
Scientist QC LC-MS Biologics(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior Labortechniker QC mit dem Schwerpunkt Bioanalytik(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QC Deviation & Investigation Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Laborant/in Quality Control(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - CH12 Lonza AG
Associate Process Chemist(m/w/x)
Vollzeitnur vor OrtManagementVisp