AbbVie
Scientist I/II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtSenior
Ludwigshafen am Rhein
Neuer Job?Nejo!
Dein persönlicher KI-Karriere-Agent
ABAbbVie
Senior Scientist II for Extractables and Leachables - PDS&T - Global Material and Parenteral Packaging Sciences(m/w/x)
Ludwigshafen am Rhein
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Evaluating extractables and leachables for sterile dosage forms and process equipment. PhD with 4+ years experience in analytical chemistry or material sciences required. 6 weeks vacation, company car for private use.
Anforderungen
- Bachelor's degree or equivalent education and 12 years of experience
- Master's degree or equivalent education and 10 years of experience
- PhD and 4 years of experience
- Degree in Analytical Chemistry, Material Sciences, Chemistry, Physic, or related fields
- Professional training substituted for equivalent work experience
- Experience in analytical method development and validation
- Adherence to USP, ICH or other compendial/regulatory requirements
- Experience with polymers and material selection
- Experience with process equipment, container closure systems, and/or medical devices
- Excellent oral communication skills
- Sound technical writing and documentation competencies
- Ability to work independently
- Ability to respond to changing priorities and short lead times
- Ability to identify problems and work toward solutions
- Ability to influence without direct authority in multi-disciplinary teams
- Attentiveness to details
- Excellent organization skills
Aufgaben
- Lead development of innovative materials and packaging solutions for sterile dosage forms
- Evaluate packaging materials and systems for sterile dosage forms
- Assess E&L, elemental impurities, and compatibility for sterile dosage forms
- Apply expert knowledge to E&L evaluation of container closure systems
- Evaluate E&L for process equipment materials for pharmaceutical products
- Provide scientific advice for E&L evaluations of process equipment
- Provide scientific advice for CCS development
- Assist with quality and regulatory activities
- Prepare technical documents for regulatory filings
- Manage and exchange scientific knowledge on E&L
- Manage and exchange scientific knowledge on CCS characterization
- Conduct external benchmarking on E&L and CCS characterization
- Prepare scientific and technical documents
- Review scientific and technical documents
- Prepare E&L study protocols and reports
- Review E&L study protocols and reports
- Prepare validation protocols and reports
- Review validation protocols and reports
- Prepare analytical test procedures
- Review analytical test procedures
- Prepare development reports
- Review development reports
- Prepare design history files
- Review design history files
- Prepare documents for CMC submissions
- Review documents for CMC submissions
- Represent the function on cross-functional project teams
- Collaborate with colleagues across development
- Collaborate with colleagues across quality
- Collaborate with colleagues across regulatory
- Collaborate with colleagues across manufacturing
- Engage with external partners and suppliers
- Contribute to internal innovation initiatives
- Participate in external scientific consortia
- Participate in external industry consortia
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- USP
- ICH
Benefits
Attraktive Vergütung
- Attractive salary
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Mentoring & Coaching
- Intensive onboarding process
- Mentor support
Flexibles Arbeiten
- Flexible work models
- Healthy work-life balance
Gesundheits- & Fitnessangebote
- Corporate health management
- Health programs
- Exercise programs
Sonstige Vorteile
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion
- Dignity and respect for employees
- Individual contributions valued
Karriere- und Weiterentwicklung
- Wide career opportunities
- Attractive development opportunities
- Strong international network
Fokus auf Nachhaltigkeit
- Environmental and community focus
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens AbbVie 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?
- AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein
ABAbbVie
Senior Scientist II for Extractables and Leachables - PDS&T - Global Material and Parenteral Packaging Sciences(m/w/x)
Ludwigshafen am Rhein
VollzeitVor OrtSenior
Nejo KI-Zusammenfassung
Evaluating extractables and leachables for sterile dosage forms and process equipment. PhD with 4+ years experience in analytical chemistry or material sciences required. 6 weeks vacation, company car for private use.
Anforderungen
- Bachelor's degree or equivalent education and 12 years of experience
- Master's degree or equivalent education and 10 years of experience
- PhD and 4 years of experience
- Degree in Analytical Chemistry, Material Sciences, Chemistry, Physic, or related fields
- Professional training substituted for equivalent work experience
- Experience in analytical method development and validation
- Adherence to USP, ICH or other compendial/regulatory requirements
- Experience with polymers and material selection
- Experience with process equipment, container closure systems, and/or medical devices
- Excellent oral communication skills
- Sound technical writing and documentation competencies
- Ability to work independently
- Ability to respond to changing priorities and short lead times
- Ability to identify problems and work toward solutions
- Ability to influence without direct authority in multi-disciplinary teams
- Attentiveness to details
- Excellent organization skills
Aufgaben
- Lead development of innovative materials and packaging solutions for sterile dosage forms
- Evaluate packaging materials and systems for sterile dosage forms
- Assess E&L, elemental impurities, and compatibility for sterile dosage forms
- Apply expert knowledge to E&L evaluation of container closure systems
- Evaluate E&L for process equipment materials for pharmaceutical products
- Provide scientific advice for E&L evaluations of process equipment
- Provide scientific advice for CCS development
- Assist with quality and regulatory activities
- Prepare technical documents for regulatory filings
- Manage and exchange scientific knowledge on E&L
- Manage and exchange scientific knowledge on CCS characterization
- Conduct external benchmarking on E&L and CCS characterization
- Prepare scientific and technical documents
- Review scientific and technical documents
- Prepare E&L study protocols and reports
- Review E&L study protocols and reports
- Prepare validation protocols and reports
- Review validation protocols and reports
- Prepare analytical test procedures
- Review analytical test procedures
- Prepare development reports
- Review development reports
- Prepare design history files
- Review design history files
- Prepare documents for CMC submissions
- Review documents for CMC submissions
- Represent the function on cross-functional project teams
- Collaborate with colleagues across development
- Collaborate with colleagues across quality
- Collaborate with colleagues across regulatory
- Collaborate with colleagues across manufacturing
- Engage with external partners and suppliers
- Contribute to internal innovation initiatives
- Participate in external scientific consortia
- Participate in external industry consortia
Berufserfahrung
- 4 Jahre
Ausbildung
- Bachelor-AbschlussODER
- Master-Abschluss
Sprachen
- Englisch – verhandlungssicher
Tools & Technologien
- USP
- ICH
Benefits
Attraktive Vergütung
- Attractive salary
Lockere Unternehmenskultur
- Diverse work environment
- Open corporate culture
- Great Place to Work recognition
- Inclusive culture
Mentoring & Coaching
- Intensive onboarding process
- Mentor support
Flexibles Arbeiten
- Flexible work models
- Healthy work-life balance
Gesundheits- & Fitnessangebote
- Corporate health management
- Health programs
- Exercise programs
Sonstige Vorteile
- Company social benefits
- International organization
- Equality, equity, diversity and inclusion
- Dignity and respect for employees
- Individual contributions valued
Karriere- und Weiterentwicklung
- Wide career opportunities
- Attractive development opportunities
- Strong international network
Fokus auf Nachhaltigkeit
- Environmental and community focus
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens AbbVie 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
AbbVie
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen setzt sich für die Entdeckung und Bereitstellung innovativer Medikamente und Lösungen ein, die ernsthafte Gesundheitsprobleme lösen.
Noch nicht perfekt?
- AbbVie
Scientist I/II(m/w/x)
VollzeitBefristeter Vertragnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Bench Scientist II / Senior Bench Scientist I – Mass Spectrometry & Characterization of Therapeutic Proteins(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein - AbbVie
Principal Research Scientist I/II / Biologics Drug Product Lead (R&D)(m/w/x)
Vollzeitnur vor OrtSeniorLudwigshafen am Rhein