Dein persönlicher KI-Karriere-Agent
Senior Principal Scientist Validation(m/w/x)
Sterilization and cleaning validation for injectable drug production. GMP operation skills and English fluency required. Company pension plan, German language skills preferred.
Anforderungen
- English fluency
- Preferred German language skills
- Engineer, pharmacist, or equivalent degree/certification/training/experience
- Professional experience in the industry
- Knowledge of GMP Operation skills
- Good document and project management skills
- German language knowledge
- Basic English knowledge
- Parenteral manufacturing knowledge
- Strong analytical and synthesis skills
- Excellent interpersonal and communication skills
- Ability to work independently
- Ability to work in a team
- Ability to coordinate teams without direct hierarchical power
Aufgaben
- Instruct and support production equipment validation
- Support system validation
- Perform sterilization validation
- Perform cleaning validation
- Perform filter validation
- Perform shipping validation
- Perform process validation
- Conduct other TS/MS related activities
- Prepare technical documents
- Review technical documents
- Prepare change controls
- Review change controls
- Prepare regulatory submissions
- Review regulatory submissions
- Prepare deviation investigations
- Review deviation investigations
- Prepare validation protocols
- Review validation protocols
- Prepare validation summary reports
- Review validation summary reports
- Prepare processing records
- Review processing records
- Prepare procedures
- Review procedures
- Participate in process functional teams
- Implement TS/MS objectives
- Deliver on business objectives
- Deliver on quality objectives
- Initiate validation protocols
- Initiate validation reports
- Coordinate validation activities
- Complete required trainings on time
- Complete assigned trainings on time
- Ensure compliance with final objective
- Coordinate with local project team
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Betriebliche Altersvorsorge
- Company pension plan
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Noch nicht perfekt?
- 350 Lilly Deutschland GmbHVollzeitnur vor OrtSeniorAlzey
- Lilly Deutschland GmbH
Senior/Principal Scientist Tech Transfer(m/w/x)
Vollzeitnur vor OrtSeniorAlzey - Lilly
Senior Principal Scientist – Sterility Assurance - Technical Services/Manufacturing Science(m/w/x)
Vollzeitnur vor OrtManagementAlzey - 350 Lilly Deutschland GmbH
Senior Quality Scientist, Device Assembly and Packaging(m/w/x)
Vollzeitnur vor OrtSeniorAlzey - 350 Lilly Deutschland GmbH
Principal Scientist - Quality Control Chemical Testing Lab(m/w/x)
Vollzeitnur vor OrtManagementAlzey
Senior Principal Scientist Validation(m/w/x)
Sterilization and cleaning validation for injectable drug production. GMP operation skills and English fluency required. Company pension plan, German language skills preferred.
Anforderungen
- English fluency
- Preferred German language skills
- Engineer, pharmacist, or equivalent degree/certification/training/experience
- Professional experience in the industry
- Knowledge of GMP Operation skills
- Good document and project management skills
- German language knowledge
- Basic English knowledge
- Parenteral manufacturing knowledge
- Strong analytical and synthesis skills
- Excellent interpersonal and communication skills
- Ability to work independently
- Ability to work in a team
- Ability to coordinate teams without direct hierarchical power
Aufgaben
- Instruct and support production equipment validation
- Support system validation
- Perform sterilization validation
- Perform cleaning validation
- Perform filter validation
- Perform shipping validation
- Perform process validation
- Conduct other TS/MS related activities
- Prepare technical documents
- Review technical documents
- Prepare change controls
- Review change controls
- Prepare regulatory submissions
- Review regulatory submissions
- Prepare deviation investigations
- Review deviation investigations
- Prepare validation protocols
- Review validation protocols
- Prepare validation summary reports
- Review validation summary reports
- Prepare processing records
- Review processing records
- Prepare procedures
- Review procedures
- Participate in process functional teams
- Implement TS/MS objectives
- Deliver on business objectives
- Deliver on quality objectives
- Initiate validation protocols
- Initiate validation reports
- Coordinate validation activities
- Complete required trainings on time
- Complete assigned trainings on time
- Ensure compliance with final objective
- Coordinate with local project team
Berufserfahrung
- 5 Jahre
Ausbildung
- Abgeschlossene BerufsausbildungODER
- Bachelor-Abschluss
Sprachen
- Englisch – verhandlungssicher
- Deutsch – verhandlungssicher
Benefits
Betriebliche Altersvorsorge
- Company pension plan
Gefällt dir diese Stelle?
BetaDein Career Agent findet täglich ähnliche Jobs für dich.
Über das Unternehmen
Lilly Deutschland GmbH
Branche
Pharmaceuticals
Beschreibung
Das Unternehmen ist ein globaler Marktführer im Gesundheitswesen mit Fokus auf die Entwicklung lebensverändernder Medikamente.
Noch nicht perfekt?
- 350 Lilly Deutschland GmbH
Senior/Principal Scientist Validation(m/w/x)
Vollzeitnur vor OrtSeniorAlzey - Lilly Deutschland GmbH
Senior/Principal Scientist Tech Transfer(m/w/x)
Vollzeitnur vor OrtSeniorAlzey - Lilly
Senior Principal Scientist – Sterility Assurance - Technical Services/Manufacturing Science(m/w/x)
Vollzeitnur vor OrtManagementAlzey - 350 Lilly Deutschland GmbH
Senior Quality Scientist, Device Assembly and Packaging(m/w/x)
Vollzeitnur vor OrtSeniorAlzey - 350 Lilly Deutschland GmbH
Principal Scientist - Quality Control Chemical Testing Lab(m/w/x)
Vollzeitnur vor OrtManagementAlzey