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
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Noch nicht perfekt?
- Bavarian Nordic GmbHVollzeitmit HomeofficeSeniorBern
- Bavarian Nordic Berna GmbH
Senior QA Manager, QV & CSV(m/w/x)
Vollzeitmit HomeofficeManagementBern - Bavarian Nordic Berna GmbH
Validation Engineer in MSAT(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBern - Bavarian Nordic Berna GmbH
Head of Global Quality Systems(m/w/x)
Vollzeitmit HomeofficeSeniorBern - Bavarian Nordic GmbH
Demand and Supply Planner(m/w/x)
Vollzeitmit HomeofficeSeniorBern
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
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
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 GmbH
QA Senior Specialist – Audit & Inspection(m/w/x)
Vollzeitmit HomeofficeSeniorBern - Bavarian Nordic Berna GmbH
Senior QA Manager, QV & CSV(m/w/x)
Vollzeitmit HomeofficeManagementBern - Bavarian Nordic Berna GmbH
Validation Engineer in MSAT(m/w/x)
Vollzeitmit HomeofficeBerufserfahrenBern - Bavarian Nordic Berna GmbH
Head of Global Quality Systems(m/w/x)
Vollzeitmit HomeofficeSeniorBern - Bavarian Nordic GmbH
Demand and Supply Planner(m/w/x)
Vollzeitmit HomeofficeSeniorBern