Lonza
MSAT Expert Drug Product(m/w/x)
Vollzeitnur vor OrtBerufserfahren
Visp
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
TEten23 health
MSAT Material Lead(m/w/x)
Visp
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Monitoring injectable medicine material quality and risks at a pharmaceutical development and manufacturing partner. GMP environment background and ERP system experience required. Flexible working arrangements, career development opportunity.
Anforderungen
- Degree in scientific, technical, or pharmaceutical field
- GMP environment background (QC, QA, Supply Chain, Material Management)
- Material/supplier qualification knowledge and regulatory requirements
- Strong awareness of quality and risk
- Experienced with ERP systems (Microsoft Dynamics)
- Master data processes experience
- Proficient use of core quality tools (Deviation Management, CAPA, Change Control)
- Structured and analytical working style
- Resilience and competence to solve complex problems
- Ability to work in a dynamic environment
- Confident communication with stakeholders
- Strong team orientation
- Assertiveness
- Deep sense of responsibility
Aufgaben
- Assess and monitor material quality and risks
- Ensure compliance with regulatory requirements
- Maintain material data in ERP system
- Initiate actions for quality issues
- Communicate with suppliers and customers
- Define quality requirements with QC and Development
- Evaluate new materials for aseptic processes
- Resolve complex quality deviations
- Link material attributes to process performance
- Lead supplier qualification and audits
- Participate in annual supplier reviews
- Implement quality-related CAPAs
- Provide material expertise to internal and external teams
- Support material-related inquiries
- Ensure transparent and compliant documentation
- Maintain material master records
- Coordinate onboarding of new materials
- Conduct root cause analyses
- Drive CAPA processes to resolution
- Create and maintain risk-analytical documents
- Guide material updates through change control
- Initiate strategic improvement measures
- Develop material specification frameworks
- Contribute to cross-site standardization
- Enhance material quality and supplier performance
- Improve production safety
Berufserfahrung
- 2 - 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Dynamics
- Deviation Management
- CAPA
- Change Control
Benefits
Karriere- und Weiterentwicklung
- Career development opportunity
Flexibles Arbeiten
- Flexible working arrangements
- Flexibility
Lockere Unternehmenskultur
- Open culture
- Diverse workforce
- Minimal bureaucracy
Mentoring & Coaching
- Learning from experienced employees
Weiterbildungsangebote
- Wide range of training options
Betriebliche Altersvorsorge
- Competitive pension fund plan
Boni & Prämien
- Annual bonus
Sonstige Vorteile
- Other financial and non-financial benefits
- Mutual trust
Sinnstiftende Arbeit
- Self-responsibility
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens ten23 health erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Noch nicht perfekt?
- Lonza
QC Raw Material Specialist(m/w/x)
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Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - ten23 health
Experienced Qualification Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
MPL Material Project Lead(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp
TEten23 health
MSAT Material Lead(m/w/x)
Visp
VollzeitVor OrtBerufserfahren
Nejo KI-Zusammenfassung
Monitoring injectable medicine material quality and risks at a pharmaceutical development and manufacturing partner. GMP environment background and ERP system experience required. Flexible working arrangements, career development opportunity.
Anforderungen
- Degree in scientific, technical, or pharmaceutical field
- GMP environment background (QC, QA, Supply Chain, Material Management)
- Material/supplier qualification knowledge and regulatory requirements
- Strong awareness of quality and risk
- Experienced with ERP systems (Microsoft Dynamics)
- Master data processes experience
- Proficient use of core quality tools (Deviation Management, CAPA, Change Control)
- Structured and analytical working style
- Resilience and competence to solve complex problems
- Ability to work in a dynamic environment
- Confident communication with stakeholders
- Strong team orientation
- Assertiveness
- Deep sense of responsibility
Aufgaben
- Assess and monitor material quality and risks
- Ensure compliance with regulatory requirements
- Maintain material data in ERP system
- Initiate actions for quality issues
- Communicate with suppliers and customers
- Define quality requirements with QC and Development
- Evaluate new materials for aseptic processes
- Resolve complex quality deviations
- Link material attributes to process performance
- Lead supplier qualification and audits
- Participate in annual supplier reviews
- Implement quality-related CAPAs
- Provide material expertise to internal and external teams
- Support material-related inquiries
- Ensure transparent and compliant documentation
- Maintain material master records
- Coordinate onboarding of new materials
- Conduct root cause analyses
- Drive CAPA processes to resolution
- Create and maintain risk-analytical documents
- Guide material updates through change control
- Initiate strategic improvement measures
- Develop material specification frameworks
- Contribute to cross-site standardization
- Enhance material quality and supplier performance
- Improve production safety
Berufserfahrung
- 2 - 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Dynamics
- Deviation Management
- CAPA
- Change Control
Benefits
Karriere- und Weiterentwicklung
- Career development opportunity
Flexibles Arbeiten
- Flexible working arrangements
- Flexibility
Lockere Unternehmenskultur
- Open culture
- Diverse workforce
- Minimal bureaucracy
Mentoring & Coaching
- Learning from experienced employees
Weiterbildungsangebote
- Wide range of training options
Betriebliche Altersvorsorge
- Competitive pension fund plan
Boni & Prämien
- Annual bonus
Sonstige Vorteile
- Other financial and non-financial benefits
- Mutual trust
Sinnstiftende Arbeit
- Self-responsibility
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens ten23 health erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
Über das Unternehmen
ten23 health
Branche
Pharmaceuticals
Beschreibung
The company is a human-centric strategic partner for the pharmaceutical industry and biotech start-ups, focusing on the development and testing of medicines.
Noch nicht perfekt?
- Lonza
MSAT Expert Drug Product(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - Lonza
QC Raw Material Specialist(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Senior QA Specialist(m/w/x)
Vollzeitnur vor OrtSeniorVisp - ten23 health
Experienced Qualification Engineer(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
MPL Material Project Lead(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp