Die KI-Suchmaschine für Jobs
QC Raw Material Specialist(m/w/x)
Beschreibung
In this Visp-based role, you will drive the quality and compliance of raw materials by leading cross-functional projects and coordinating complex approval workflows across the laboratories.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •PhD or equivalent Life Sciences experience
- •Advantageous pharmaceutical, biotechnological GMP, or QC experience
- •Proficient use of MS Office
- •Advantageous pharmaceutical or laboratory software knowledge
- •Enjoyment of cross-functional collaboration
- •Organizational and project management skills
- •Integrity and assertiveness in communication
- •Excellent English communication skills
- •Advantageous German communication skills
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Lead QC projects in cross-functional teams
- •Collaborate with labs, program management, and production
- •Coordinate material onboarding with procurement and supply chain
- •Manage material evaluation and approval workflows
- •Track testing and documentation for material qualification
- •Facilitate laboratory analyses and project approvals
- •Prepare reports to improve product quality
- •Plan and supervise experimental laboratory work
- •Develop specifications and handling instructions for materials
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- •High performance compensation programs
Karriere- und Weiterentwicklung
- •Agile career
Lockere Unternehmenskultur
- •Dynamic working culture
Sinnstiftende Arbeit
- •Inclusive and ethical workplace
Sonstige Vorteile
- •Relocation assistance
- LonzaVollzeitnur vor OrtBerufserfahrenVisp
- Lonza
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Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QA Specialist, Batch Record Review(m/w/x)
Vollzeitnur vor OrtJuniorVisp
QC Raw Material Specialist(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this Visp-based role, you will drive the quality and compliance of raw materials by leading cross-functional projects and coordinating complex approval workflows across the laboratories.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •PhD or equivalent Life Sciences experience
- •Advantageous pharmaceutical, biotechnological GMP, or QC experience
- •Proficient use of MS Office
- •Advantageous pharmaceutical or laboratory software knowledge
- •Enjoyment of cross-functional collaboration
- •Organizational and project management skills
- •Integrity and assertiveness in communication
- •Excellent English communication skills
- •Advantageous German communication skills
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Lead QC projects in cross-functional teams
- •Collaborate with labs, program management, and production
- •Coordinate material onboarding with procurement and supply chain
- •Manage material evaluation and approval workflows
- •Track testing and documentation for material qualification
- •Facilitate laboratory analyses and project approvals
- •Prepare reports to improve product quality
- •Plan and supervise experimental laboratory work
- •Develop specifications and handling instructions for materials
Tools & Technologien
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- •High performance compensation programs
Karriere- und Weiterentwicklung
- •Agile career
Lockere Unternehmenskultur
- •Dynamic working culture
Sinnstiftende Arbeit
- •Inclusive and ethical workplace
Sonstige Vorteile
- •Relocation assistance
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.
- Lonza
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Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
Scientist Quality Control, Microbiology(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Vollzeitnur vor OrtSeniorVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - Lonza
QA Specialist, Batch Record Review(m/w/x)
Vollzeitnur vor OrtJuniorVisp