Catalent, Inc.
Teamleiter pharmazeutische Produktion(m/w/x)
Full-timeOn-siteSenior
Eberbach
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CACatalent
Head of Production - Finishing(m/w/x)
Eberbach
Full-timeOn-siteSenior
Nejo AI Summary
Leading GMP-compliant drug dosage form finishing, overseeing visual inspection, packaging, coating, and hardening with 100+ employees at global drug developer. Pharmaceutical/GMP manufacturing experience and leadership of large shift-based teams required. Disability accommodations provided.
Requirements
- Degree in Pharmacy, Chemistry, Engineering, or related field
- Experience in pharmaceutical or GMP-regulated production
- Leadership experience managing large shift-based teams
- Experience with Lean Management and continuous improvement
- Understanding of GMP regulations and compliance
- Knowledge of production processes in GMP environment
- Familiarity with digital production management tools
- Ability to analyze KPIs and data
- Understanding of quality assurance and regulations
- Strong leadership and people management skills
- Change management mindset
- Customer orientation and Patient First commitment
- Excellent communication and decision-making abilities
- Ability to manage complex operations under pressure
- Strategic thinking and hands-on problem-solving
- Fluency in German and English
- Willingness to work in shift-based environment
- Openness to digital innovation and learning
- Intercultural competence and international experience
Tasks
- Lead a GMP-compliant production area
- Manage approximately 100 employees across multiple shifts
- Oversee visual inspection and bulk packaging
- Supervise blister packaging and printing processes
- Manage product treatments like coating and hardening
- Ensure adherence to global quality standards
- Implement Lean Management to optimize efficiency
- Monitor production KPIs and initiate corrective actions
- Coordinate with Quality Assurance and Supply Chain
- Drive digitalization and process optimization projects
- Ensure staff training and GMP qualification
- Manage budgets and resource capacity planning
- Handle regulatory and customer audits
- Execute special projects for senior management
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Lean Management
- KPIs
Benefits
Career Advancement
- Career advancement opportunities
Other Benefits
- Disability accommodations
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Catalent 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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CACatalent
Head of Production - Finishing(m/w/x)
Eberbach
Full-timeOn-siteSenior
Nejo AI Summary
Leading GMP-compliant drug dosage form finishing, overseeing visual inspection, packaging, coating, and hardening with 100+ employees at global drug developer. Pharmaceutical/GMP manufacturing experience and leadership of large shift-based teams required. Disability accommodations provided.
Requirements
- Degree in Pharmacy, Chemistry, Engineering, or related field
- Experience in pharmaceutical or GMP-regulated production
- Leadership experience managing large shift-based teams
- Experience with Lean Management and continuous improvement
- Understanding of GMP regulations and compliance
- Knowledge of production processes in GMP environment
- Familiarity with digital production management tools
- Ability to analyze KPIs and data
- Understanding of quality assurance and regulations
- Strong leadership and people management skills
- Change management mindset
- Customer orientation and Patient First commitment
- Excellent communication and decision-making abilities
- Ability to manage complex operations under pressure
- Strategic thinking and hands-on problem-solving
- Fluency in German and English
- Willingness to work in shift-based environment
- Openness to digital innovation and learning
- Intercultural competence and international experience
Tasks
- Lead a GMP-compliant production area
- Manage approximately 100 employees across multiple shifts
- Oversee visual inspection and bulk packaging
- Supervise blister packaging and printing processes
- Manage product treatments like coating and hardening
- Ensure adherence to global quality standards
- Implement Lean Management to optimize efficiency
- Monitor production KPIs and initiate corrective actions
- Coordinate with Quality Assurance and Supply Chain
- Drive digitalization and process optimization projects
- Ensure staff training and GMP qualification
- Manage budgets and resource capacity planning
- Handle regulatory and customer audits
- Execute special projects for senior management
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- German – Business Fluent
- English – Business Fluent
Tools & Technologies
- Lean Management
- KPIs
Benefits
Career Advancement
- Career advancement opportunities
Other Benefits
- Disability accommodations
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Catalent 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.
About the Company
Catalent
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein globaler Marktführer in der Entwicklung von Darreichungsformen von Medikamenten und bietet über 7.000 Produkte an.
Not a perfect match?
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