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Principal Associate Scientist(m/w/x)
Beschreibung
In this role, you will engage in routine analyses and method development, ensuring quality assessments of active substances while collaborating with various teams to support both research and commercial manufacturing efforts.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Apprenticeship or Bachelor/Master in life sciences
- •At least 10 years of experience in an industrial setting
- •Experience working on bioassays
- •Experience in a QC organization
- •Experience working according to GMP
- •Strong hands-on experience in immunological methodologies
- •Experience with ELISA, reporter gene assays, proliferation assays, cell killing assays, and cell culture
- •Self-organizing way of working
- •Ability to interact and cooperate across matrix organizations
- •Good written and spoken English
- •Knowledge of German is a big advantage
Ausbildung
Berufserfahrung
10 Jahre
Aufgaben
- •Conduct routine analysis of release and stability samples
- •Perform extended functional characterization across multiple projects
- •Follow GMP compliant workflows in the analytical landscape
- •Develop and validate analytical methods for quality assessment
- •Support interfaces with early research and development
- •Collaborate with the marketed QC organization
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
- CH12 Lonza AGVollzeitnur vor OrtSeniorBasel, Stein (AR)
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Senior GMP Validation Scientist – Laboratory Execution Physico-Chemical Quality Control(m/w/x)
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Group Head in Analytical Development & Quality Control(m/w/x)
Vollzeitnur vor OrtManagementBasel
Principal Associate Scientist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will engage in routine analyses and method development, ensuring quality assessments of active substances while collaborating with various teams to support both research and commercial manufacturing efforts.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Apprenticeship or Bachelor/Master in life sciences
- •At least 10 years of experience in an industrial setting
- •Experience working on bioassays
- •Experience in a QC organization
- •Experience working according to GMP
- •Strong hands-on experience in immunological methodologies
- •Experience with ELISA, reporter gene assays, proliferation assays, cell killing assays, and cell culture
- •Self-organizing way of working
- •Ability to interact and cooperate across matrix organizations
- •Good written and spoken English
- •Knowledge of German is a big advantage
Ausbildung
Berufserfahrung
10 Jahre
Aufgaben
- •Conduct routine analysis of release and stability samples
- •Perform extended functional characterization across multiple projects
- •Follow GMP compliant workflows in the analytical landscape
- •Develop and validate analytical methods for quality assessment
- •Support interfaces with early research and development
- •Collaborate with the marketed QC organization
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Über das Unternehmen
1201 F. Hoffmann-La Roche AG
Branche
Pharmaceuticals
Beschreibung
Roche is dedicated to advancing science and ensuring access to healthcare for everyone, with over 100,000 employees globally.
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Senior GMP Validation Scientist – Laboratory Execution Physico-Chemical Quality Control(m/w/x)
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Group Head in Analytical Development & Quality Control(m/w/x)
Vollzeitnur vor OrtManagementBasel