Dein persönlicher KI-Karriere-Agent
Scientist QC for Stability Programs(m/w/x)
Managing stability study initiation, planning, sample management, and reporting for vaccines. 5+ years pharmaceutical QC experience in cGMP biotechnology required. Support for personal and academic skills growth.
Anforderungen
- University degree in natural science
- 5+ years pharmaceutical industry experience
- Focus on quality control and biotechnology in cGMP
- Expertise in stability studies for drug substances
- Expertise in stability studies for drug products
- Knowledge of relevant regulatory requirements
- Experience supporting Health Authority inspections
- Experience participating in Health Authority inspections
- Ability to manage complex programs
- High motivation and ownership
- Strong organizational and planning skills
- Ability to prioritize effectively
- Ability to meet deadlines
- Collaborative mindset
- Ability to build effective working relationships
- Ability to drive solutions
- Proficiency in German
- Proficiency in English
Aufgaben
- Act as stability program subject matter expert
- Manage local stability study process
- Coordinate stability study initiation, planning, sample management, and reporting
- Monitor and ensure timely execution of stability studies
- Analyze and interpret stability data and reports
- Support decision-making with stability data
- Ensure compliance and inspection readiness of stability programs
- Maintain stability program infrastructure
- Represent stability program during inspections
- Collaborate cross-functionally and across sites
- Harmonize and optimize stability processes
- Contribute to scientific and statistical standards for stability programs
- Support product teams with stability-related activities
- Assist with submissions, program changes, and clinical trial materials
- Provide justification for product shelf life
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Mentoring & Coaching
- Support for personal and academic skills growth
Noch nicht perfekt?
- Bavarian Nordic Berna GmbHVollzeitmit HomeofficeManagementBern
- Bavarian Nordic GmbH
Demand and Supply Planner(m/w/x)
Vollzeitmit HomeofficeSeniorBern - Bavarian Nordic Berna GmbH
MSAT Trainee(m/w/x)
VollzeitBefristeter Vertragmit HomeofficeJuniorBern - Bavarian Nordic Berna GmbH
S&OE Coordinator(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBern - Bavarian Nordic Berna GmbH
Sales Force & Omnichannel Data Analytics Lead(m/w/x)
VollzeitRemoteBerufserfahrenBern
Scientist QC for Stability Programs(m/w/x)
Managing stability study initiation, planning, sample management, and reporting for vaccines. 5+ years pharmaceutical QC experience in cGMP biotechnology required. Support for personal and academic skills growth.
Anforderungen
- University degree in natural science
- 5+ years pharmaceutical industry experience
- Focus on quality control and biotechnology in cGMP
- Expertise in stability studies for drug substances
- Expertise in stability studies for drug products
- Knowledge of relevant regulatory requirements
- Experience supporting Health Authority inspections
- Experience participating in Health Authority inspections
- Ability to manage complex programs
- High motivation and ownership
- Strong organizational and planning skills
- Ability to prioritize effectively
- Ability to meet deadlines
- Collaborative mindset
- Ability to build effective working relationships
- Ability to drive solutions
- Proficiency in German
- Proficiency in English
Aufgaben
- Act as stability program subject matter expert
- Manage local stability study process
- Coordinate stability study initiation, planning, sample management, and reporting
- Monitor and ensure timely execution of stability studies
- Analyze and interpret stability data and reports
- Support decision-making with stability data
- Ensure compliance and inspection readiness of stability programs
- Maintain stability program infrastructure
- Represent stability program during inspections
- Collaborate cross-functionally and across sites
- Harmonize and optimize stability processes
- Contribute to scientific and statistical standards for stability programs
- Support product teams with stability-related activities
- Assist with submissions, program changes, and clinical trial materials
- Provide justification for product shelf life
Berufserfahrung
- 5 Jahre
Ausbildung
- Bachelor-Abschluss
Sprachen
- Deutsch – verhandlungssicher
- Englisch – verhandlungssicher
Benefits
Mentoring & Coaching
- Support for personal and academic skills growth
Über das Unternehmen
Bavarian Nordic 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
Senior QA Manager, QV & CSV(m/w/x)
Vollzeitmit HomeofficeManagementBern - Bavarian Nordic GmbH
Demand and Supply Planner(m/w/x)
Vollzeitmit HomeofficeSeniorBern - Bavarian Nordic Berna GmbH
MSAT Trainee(m/w/x)
VollzeitBefristeter Vertragmit HomeofficeJuniorBern - Bavarian Nordic Berna GmbH
S&OE Coordinator(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBern - Bavarian Nordic Berna GmbH
Sales Force & Omnichannel Data Analytics Lead(m/w/x)
VollzeitRemoteBerufserfahrenBern