350 Lilly Deutschland GmbH
Senior/Principal Scientist Validation(m/w/x)
Full-timeOn-siteSenior
Alzey
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LILilly Deutschland GmbH
Senior Principal Scientist Validation(m/w/x)
Alzey
Full-timeOn-siteSenior
Nejo AI Summary
Sterilization and cleaning validation for injectable drug production. GMP operation skills and English fluency required. Company pension plan, German language skills preferred.
Requirements
- 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
Tasks
- 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
Work Experience
- 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Retirement Plans
- Company pension plan
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lilly Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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LILilly Deutschland GmbH
Senior Principal Scientist Validation(m/w/x)
Alzey
Full-timeOn-siteSenior
Nejo AI Summary
Sterilization and cleaning validation for injectable drug production. GMP operation skills and English fluency required. Company pension plan, German language skills preferred.
Requirements
- 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
Tasks
- 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
Work Experience
- 5 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Retirement Plans
- Company pension plan
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Lilly Deutschland GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Lilly Deutschland GmbH
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer im Gesundheitswesen mit Fokus auf die Entwicklung lebensverändernder Medikamente.
Not a perfect match?
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