Die KI-Suchmaschine für Jobs
Manufacturing Specialist Vibe-X(m/w/x)
Beschreibung
In this role, you will be at the forefront of vaccine production, collaborating on innovative processes and ensuring compliance with GMP standards. Your day-to-day responsibilities will include executing manufacturing activities, troubleshooting equipment, and training staff, while also contributing to the setup of new production areas.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Completed chemical/biopharmaceutical education or corresponding training qualification
- •Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or several years of relevant professional experience
- •Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation, protein purification, or Bioconjugates
- •Excellent communication skills
- •Teamwork skills
- •Driven and solution-oriented attitude
- •Fluency in English
- •Fluency in German is considered a plus
- •Basic GMP understanding is a plus
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Support the project team in defining innovative vaccine production processes
- •Collaborate on qualifying and validating new production areas and processes
- •Execute manufacturing activities in Upstream Processing, Downstream Processing, or Bioconjugates according to cGMP and SOPs
- •Evaluate test results and troubleshoot manufacturing equipment
- •Make recommendations for resolving manufacturing issues
- •Prepare risk assessments for Safety, Health, Environment, and Environmental Monitoring
- •Assist in preparing documents like electronic batch records and SOPs for the production area
- •Review production documentation and address deviations and change requests
- •Implement CAPAs to maintain high-quality GMP standards
- •Engage in capital investment projects for new manufacturing units as a manufacturing expert
- •Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- •Train manufacturing staff on specific equipment and standard operations
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Sonstige Zulagen
- •Relocation assistance for eligible candidates
- CH12 Lonza AGVollzeitnur vor OrtBerufserfahrenVisp
- CH12 Lonza AG
Manufacturing Specialist Mammalian(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - Lonza
Manufacturing Specialist, BMS(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Manufacturing Specialist(m/w/x)
Vollzeitnur vor OrtJuniorVisp - CH12 Lonza AG
Manufacturing Specialist Mammalian 100%(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp
Manufacturing Specialist Vibe-X(m/w/x)
Die KI-Suchmaschine für Jobs
Beschreibung
In this role, you will be at the forefront of vaccine production, collaborating on innovative processes and ensuring compliance with GMP standards. Your day-to-day responsibilities will include executing manufacturing activities, troubleshooting equipment, and training staff, while also contributing to the setup of new production areas.
Lass KI die perfekten Jobs für dich finden!
Lade deinen CV hoch und die Nejo-KI findet passende Stellenangebote für dich.
Anforderungen
- •Completed chemical/biopharmaceutical education or corresponding training qualification
- •Bachelor/Master's degree in Biotechnology, Biology, Biochemical Engineering or several years of relevant professional experience
- •Sound knowledge of biotechnological processes in microbial and/or mammalian cultivation, protein purification, or Bioconjugates
- •Excellent communication skills
- •Teamwork skills
- •Driven and solution-oriented attitude
- •Fluency in English
- •Fluency in German is considered a plus
- •Basic GMP understanding is a plus
Ausbildung
Berufserfahrung
ca. 1 - 4 Jahre
Aufgaben
- •Support the project team in defining innovative vaccine production processes
- •Collaborate on qualifying and validating new production areas and processes
- •Execute manufacturing activities in Upstream Processing, Downstream Processing, or Bioconjugates according to cGMP and SOPs
- •Evaluate test results and troubleshoot manufacturing equipment
- •Make recommendations for resolving manufacturing issues
- •Prepare risk assessments for Safety, Health, Environment, and Environmental Monitoring
- •Assist in preparing documents like electronic batch records and SOPs for the production area
- •Review production documentation and address deviations and change requests
- •Implement CAPAs to maintain high-quality GMP standards
- •Engage in capital investment projects for new manufacturing units as a manufacturing expert
- •Deliver input for the setup, commissioning, and qualification of manufacturing suites and equipment
- •Train manufacturing staff on specific equipment and standard operations
Sprachen
Englisch – verhandlungssicher
Deutsch – Grundkenntnisse
Benefits
Sonstige Zulagen
- •Relocation assistance for eligible candidates
Über das Unternehmen
CH12 Lonza AG
Branche
Pharmaceuticals
Beschreibung
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
- CH12 Lonza AG
Manufacturing Specialist BioConjugates(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Manufacturing Specialist Mammalian(m/w/x)
Vollzeitnur vor OrtKeine AngabeVisp - Lonza
Manufacturing Specialist, BMS(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp - CH12 Lonza AG
Manufacturing Specialist(m/w/x)
Vollzeitnur vor OrtJuniorVisp - CH12 Lonza AG
Manufacturing Specialist Mammalian 100%(m/w/x)
Vollzeitnur vor OrtBerufserfahrenVisp