Dein persönlicher KI-Karriere-Agent
QA Specialist – CSV & QV(m/w/x)
Leading Computer System Validation (CSV) and Qualification/Validation (QV) for mpox, smallpox, and travel vaccines. 5+ years of CSV experience in regulated industries required. Exceptional technology, vibrant work environment.
Anforderungen
- University degree in engineering, life sciences, computer science, or related field
- Minimum 5 years of experience in CSV and ideally QV within pharmaceutical, biotechnology, or related regulated industry; QA experience is a plus
- Capability to drive and coordinate complex validation projects in cross-functional environment with multiple stakeholders
- In-depth knowledge of cGMP, GAMP, FDA, EMA, and other relevant regulations and guidelines
- Strong technical writing, problem-solving, and project management skills
- Excellent written and spoken English skills; German is an advantage, combined with strong interpersonal and communication abilities
Aufgaben
- Ensure high quality standards for pharmaceutical products
- Lead Computer System Validation (CSV) activities
- Manage Qualification and Validation (QV) processes
- Comply with regulatory requirements and industry best practices
- Develop CSV and QV strategies, plans, protocols, and reports
- Collaborate with Engineering, Manufacturing, IT, and Quality services
- Participate in audits and inspections for CSV and QV
- Maintain robust documentation for audits and inspections
- Foster a culture of quality and continuous improvement
- Mentor team members and stakeholders
- Support changes and corrections in CSV and QV
- Act as subject matter expert for relevant regulations
- Adhere to EU GMP and FDA 21 CFR Part 11 guidelines
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- CSV
- QV
- cGMP
- GAMP
- FDA
- EMA
Benefits
Moderne Technikausstattung
- Exceptional technology
Sonstige Vorteile
- Determined team
Startup-Atmosphäre
- Vibrant and adaptable work environment
Weiterbildungsangebote
- Support for personal and professional skills growth
Noch nicht perfekt?
- Bavarian Nordic Berna GmbHVollzeitnur vor OrtBerufserfahrenBern
- Bavarian Nordic GmbH
QA Sterility Assurance Specialist(m/w/x)
Vollzeitnur vor OrtSeniorBern - Bavarian Nordic Berna GmbH
LIMS Administrator and CSV Professional(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - CSL Behring
Scientific Expert Quality Assurance 100%(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - CSL Behring
Specialist Quality Assurance 100% - Spätschicht(m/w/x)
Vollzeitnur vor OrtKeine AngabeBern
QA Specialist – CSV & QV(m/w/x)
Leading Computer System Validation (CSV) and Qualification/Validation (QV) for mpox, smallpox, and travel vaccines. 5+ years of CSV experience in regulated industries required. Exceptional technology, vibrant work environment.
Anforderungen
- University degree in engineering, life sciences, computer science, or related field
- Minimum 5 years of experience in CSV and ideally QV within pharmaceutical, biotechnology, or related regulated industry; QA experience is a plus
- Capability to drive and coordinate complex validation projects in cross-functional environment with multiple stakeholders
- In-depth knowledge of cGMP, GAMP, FDA, EMA, and other relevant regulations and guidelines
- Strong technical writing, problem-solving, and project management skills
- Excellent written and spoken English skills; German is an advantage, combined with strong interpersonal and communication abilities
Aufgaben
- Ensure high quality standards for pharmaceutical products
- Lead Computer System Validation (CSV) activities
- Manage Qualification and Validation (QV) processes
- Comply with regulatory requirements and industry best practices
- Develop CSV and QV strategies, plans, protocols, and reports
- Collaborate with Engineering, Manufacturing, IT, and Quality services
- Participate in audits and inspections for CSV and QV
- Maintain robust documentation for audits and inspections
- Foster a culture of quality and continuous improvement
- Mentor team members and stakeholders
- Support changes and corrections in CSV and QV
- Act as subject matter expert for relevant regulations
- Adhere to EU GMP and FDA 21 CFR Part 11 guidelines
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- CSV
- QV
- cGMP
- GAMP
- FDA
- EMA
Benefits
Moderne Technikausstattung
- Exceptional technology
Sonstige Vorteile
- Determined team
Startup-Atmosphäre
- Vibrant and adaptable work environment
Weiterbildungsangebote
- Support for personal and professional skills growth
Über das Unternehmen
Bavarian Nordic Berna GmbH
Branche
Pharmaceuticals
Beschreibung
The company is a global leader in developing life-saving vaccines with over 30 years of experience.
Noch nicht perfekt?
- Bavarian Nordic Berna GmbH
Quality Assurance Specialist Qualification(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - Bavarian Nordic GmbH
QA Sterility Assurance Specialist(m/w/x)
Vollzeitnur vor OrtSeniorBern - Bavarian Nordic Berna GmbH
LIMS Administrator and CSV Professional(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - CSL Behring
Scientific Expert Quality Assurance 100%(m/w/x)
Vollzeitnur vor OrtBerufserfahrenBern - CSL Behring
Specialist Quality Assurance 100% - Spätschicht(m/w/x)
Vollzeitnur vor OrtKeine AngabeBern