Bavarian Nordic GmbH
QA Sterility Assurance Specialist(m/w/x)
Vollzeitnur vor OrtSenior
Bern
Neuer Job?Nejo!
Die KI-Suchmaschine für Jobs
Driving global regulatory strategies for clinical trial applications and managing submissions for human blood plasma therapies. Sound knowledge in biological medicinal products and 5+ years biotech/pharma experience, 3+ years in Regulatory Affairs required. Global project responsibility, cross-functional collaboration.
Anforderungen
- University degree in natural sciences (BS/BA/MS or equivalent)
- Degree in Regulatory Affairs advantageous
- Minimum of 5 years’ experience in biotech or pharmaceutical industry
- At least 3 years in Regulatory Affairs
- Sound knowledge in natural sciences with focus on biological medicinal products
- Basic knowledge of regulatory framework in at least one key region (US, EU, Japan, CH, Australia)
- Excellent communication skills
- Project management skills
- Planning skills
- Problem solving skills
- Presentation skills
- Strong team player
- Ability to develop constructive relationships with peers and management
- Strong organizational skills
- Attention to detail
- Ability to work with minimal supervision
- Flexibility to work in a global cross-cultural environment
- Microsoft Office skills
- Fluency in English
- Fluency in local language
Aufgaben
- Drive global CMC strategies for clinical trial applications
- Manage regulatory submissions for new product licenses and post-approval changes
- Serve as the primary regulatory liaison with technical experts
- Support GMP inspections and ensure inspection readiness
- Interpret regulatory guidelines and prepare impact assessments
- Contribute to process improvements in regulatory activities
- Provide technical guidance to CMC Scientists
- Maintain content of relevant regulatory dossiers
- Prepare and review Module 2.3 and Module 3 documentation
- Ensure timely responses to CMC-related Health Authority questions
- Compile CMC information for CTAs, INDs, and other submissions
- Execute timely and compliant regulatory assessments for CMC changes
- Prepare CMC documentation for tenders and promotional materials
- Contribute to annual product quality reviews and risk assessments
- Participate in Global Regulatory Affairs Strategy Teams
- Represent Global Regulatory Affairs in CMC project teams
- Develop and implement global CMC regulatory strategies
- Interface with technical expert departments for project planning
- Evaluate technical CMC information for regulatory compliance
- Perform gap analysis and propose remediation strategies
- Support scheduling and prioritization of CMC submissions
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Office
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CSL Plasma 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?
- Bavarian Nordic Berna GmbH
Quality Assurance Specialist Qualification(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - Bavarian Nordic GmbH
Medical Officer(m/w/x)
Vollzeitnur vor OrtManagementBern - CSL Behring
Associate Director, Quality Assurance Support(m/w/x)
Vollzeitnur vor OrtSeniorBern - CSL Behring
Senior Production Scientist(m/w/x)
Vollzeitnur vor OrtSeniorBern
Driving global regulatory strategies for clinical trial applications and managing submissions for human blood plasma therapies. Sound knowledge in biological medicinal products and 5+ years biotech/pharma experience, 3+ years in Regulatory Affairs required. Global project responsibility, cross-functional collaboration.
Anforderungen
- University degree in natural sciences (BS/BA/MS or equivalent)
- Degree in Regulatory Affairs advantageous
- Minimum of 5 years’ experience in biotech or pharmaceutical industry
- At least 3 years in Regulatory Affairs
- Sound knowledge in natural sciences with focus on biological medicinal products
- Basic knowledge of regulatory framework in at least one key region (US, EU, Japan, CH, Australia)
- Excellent communication skills
- Project management skills
- Planning skills
- Problem solving skills
- Presentation skills
- Strong team player
- Ability to develop constructive relationships with peers and management
- Strong organizational skills
- Attention to detail
- Ability to work with minimal supervision
- Flexibility to work in a global cross-cultural environment
- Microsoft Office skills
- Fluency in English
- Fluency in local language
Aufgaben
- Drive global CMC strategies for clinical trial applications
- Manage regulatory submissions for new product licenses and post-approval changes
- Serve as the primary regulatory liaison with technical experts
- Support GMP inspections and ensure inspection readiness
- Interpret regulatory guidelines and prepare impact assessments
- Contribute to process improvements in regulatory activities
- Provide technical guidance to CMC Scientists
- Maintain content of relevant regulatory dossiers
- Prepare and review Module 2.3 and Module 3 documentation
- Ensure timely responses to CMC-related Health Authority questions
- Compile CMC information for CTAs, INDs, and other submissions
- Execute timely and compliant regulatory assessments for CMC changes
- Prepare CMC documentation for tenders and promotional materials
- Contribute to annual product quality reviews and risk assessments
- Participate in Global Regulatory Affairs Strategy Teams
- Represent Global Regulatory Affairs in CMC project teams
- Develop and implement global CMC regulatory strategies
- Interface with technical expert departments for project planning
- Evaluate technical CMC information for regulatory compliance
- Perform gap analysis and propose remediation strategies
- Support scheduling and prioritization of CMC submissions
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- Microsoft Office
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens CSL Plasma 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
CSL Plasma
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen betreibt eines der weltweit größten Netzwerke von Spendezentren für menschliches Blutplasma und stellt lebensrettende Therapien her.
Noch nicht perfekt?
- Bavarian Nordic GmbH
QA Sterility Assurance Specialist(m/w/x)
Vollzeitnur vor OrtSeniorBern - Bavarian Nordic Berna GmbH
Quality Assurance Specialist Qualification(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - Bavarian Nordic GmbH
Medical Officer(m/w/x)
Vollzeitnur vor OrtManagementBern - CSL Behring
Associate Director, Quality Assurance Support(m/w/x)
Vollzeitnur vor OrtSeniorBern - CSL Behring
Senior Production Scientist(m/w/x)
Vollzeitnur vor OrtSeniorBern