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Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Creating system specifications and conducting qualification testing for BioLife LIMS at a research-based biopharmaceutical company. 1-2 years validation experience in GMP environment with Agile methodology required. Job rotations, mentoring program.
Anforderungen
- Completed natural scientific or technical education
- At least 1-2 years experience with validation, computerized systems, and/or specifications
- Experience in GMP environment and AGILE methodology
- Very good English language skills
- Good German language skills
- Flexibility and teamwork skills
- Experience in technical and quality documentation
- Analytical thinking and problem solving
- High customer and service orientation
- Independent, precise, and methodical way of working
Aufgaben
- Create system specifications and key validation documents
- Review and approve validation documents
- Test system functionality
- Manage validation tasks and coordinate resources
- Plan and conduct qualification testing
- Evaluate test results
- Participate in designing Lab Operation processes
- Create system Standard Operating Procedures
Berufserfahrung
- 1 - 2 Jahre
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- Attractive annual bonus
Attraktive Vergütung
- Increased payment possible
Weiterbildungsangebote
- Trainings
Abwechslungsreiche Aufgaben
- Job rotations
Mentoring & Coaching
- Mentoring
Familienfreundlichkeit
- Balanced work-life ratio
Kinderbetreuung
- Company kindergarten
Gesundheits- & Fitnessangebote
- Fitness center
Gratis oder Vergünstigte Mahlzeiten
- Cafeteria
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Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Creating system specifications and conducting qualification testing for BioLife LIMS at a research-based biopharmaceutical company. 1-2 years validation experience in GMP environment with Agile methodology required. Job rotations, mentoring program.
Anforderungen
- Completed natural scientific or technical education
- At least 1-2 years experience with validation, computerized systems, and/or specifications
- Experience in GMP environment and AGILE methodology
- Very good English language skills
- Good German language skills
- Flexibility and teamwork skills
- Experience in technical and quality documentation
- Analytical thinking and problem solving
- High customer and service orientation
- Independent, precise, and methodical way of working
Aufgaben
- Create system specifications and key validation documents
- Review and approve validation documents
- Test system functionality
- Manage validation tasks and coordinate resources
- Plan and conduct qualification testing
- Evaluate test results
- Participate in designing Lab Operation processes
- Create system Standard Operating Procedures
Berufserfahrung
- 1 - 2 Jahre
Ausbildung
- Abgeschlossene Berufsausbildung
Sprachen
- Englisch – verhandlungssicher
- Deutsch – Grundkenntnisse
Benefits
Boni & Prämien
- Attractive annual bonus
Attraktive Vergütung
- Increased payment possible
Weiterbildungsangebote
- Trainings
Abwechslungsreiche Aufgaben
- Job rotations
Mentoring & Coaching
- Mentoring
Familienfreundlichkeit
- Balanced work-life ratio
Kinderbetreuung
- Company kindergarten
Gesundheits- & Fitnessangebote
- Fitness center
Gratis oder Vergünstigte Mahlzeiten
- Cafeteria
Über das Unternehmen
Takeda Manufacturing Austria AG
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein weltweit führendes, forschendes biopharmazeutisches Unternehmen, das lebensverbessernde Arzneimittel für komplexe Erkrankungen entwickelt.
Noch nicht perfekt?
- AOP Health
Application Owner (GxP / Validated Systems)(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenWienab 45.080 / Jahr - Boehringer Ingelheim
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Vollzeitmit HomeofficeBerufserfahrenWienab 3.800 / Monat - Kwizda Pharmadistribution GmbH
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Vollzeitmit HomeofficeJuniorLeopoldsdorf, Wienab 50.000 / Jahr - Galderma Austria
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