BLACKROLL AG
Senior Project Manager(m/w/x)
Full-timeWith HomeofficeSenior
Bottighofen
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EUEurofins
GMP Project Manager - Pharma(m/w/x)
Konstanz
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Leading end-to-end pharma analytics projects, including document review and stakeholder reporting. 3+ years regulated environment experience required. Partial remote work, flexible hours.
Requirements
- Degree in life sciences or vocational training in pharmaceutical/chemical field
- 3+ years relevant professional experience in regulated environment (ISO 17025, GLP, ideally GMP)
- Hands-on experience in pharmaceutical QC/analytical development
- Strong customer orientation and clear communication
- Very good IT literacy and Office skills
- LIMS experience is a plus
- Demonstrated project management capability
- Project management certification (e.g., PMP, IPMA) is an advantage
- Excellent organizational skills and prioritization
- Problem-solving in dynamic settings
- High sense of responsibility
- Reliability and team spirit
- Very good German language skills
- Good English language skills
Tasks
- Lead end-to-end Pharma Analytics projects
- Manage project planning and timelines
- Track project milestones and manage purchase orders
- Report project status to stakeholders
- Review and approve technical documents
- Ensure GMP compliance in analytical work
- Contribute to audit readiness and continuous improvement
- Configure projects in LIMS
- Support data integrity best practices
- Coordinate with internal labs, clients, and external partners
- Support new project acquisition
- Author and maintain SOPs and GMP documentation
- Support client, GMP, and regulatory audits
- Identify and implement process improvements
- Increase site efficiency, quality, and throughput
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
Tools & Technologies
- LIMS
- PMP
- IPMA
Benefits
Flexible Working
- Flexible working hours
- Partial remote work
Competitive Pay
- Competitive compensation
- Equity
Learning & Development
- Training
- Certifications
Public Transport Subsidies
- Mobility opportunities
Diverse Work
- International projects
Modern Office
- Modern workplace
Modern Equipment
- Digital collaboration
Other Benefits
- Data integrity focus
- Attractive social benefits
- Diversity
- Inclusion
Sustainability Focus
- Sustainability
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Eurofins 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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EUEurofins
GMP Project Manager - Pharma(m/w/x)
Konstanz
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Leading end-to-end pharma analytics projects, including document review and stakeholder reporting. 3+ years regulated environment experience required. Partial remote work, flexible hours.
Requirements
- Degree in life sciences or vocational training in pharmaceutical/chemical field
- 3+ years relevant professional experience in regulated environment (ISO 17025, GLP, ideally GMP)
- Hands-on experience in pharmaceutical QC/analytical development
- Strong customer orientation and clear communication
- Very good IT literacy and Office skills
- LIMS experience is a plus
- Demonstrated project management capability
- Project management certification (e.g., PMP, IPMA) is an advantage
- Excellent organizational skills and prioritization
- Problem-solving in dynamic settings
- High sense of responsibility
- Reliability and team spirit
- Very good German language skills
- Good English language skills
Tasks
- Lead end-to-end Pharma Analytics projects
- Manage project planning and timelines
- Track project milestones and manage purchase orders
- Report project status to stakeholders
- Review and approve technical documents
- Ensure GMP compliance in analytical work
- Contribute to audit readiness and continuous improvement
- Configure projects in LIMS
- Support data integrity best practices
- Coordinate with internal labs, clients, and external partners
- Support new project acquisition
- Author and maintain SOPs and GMP documentation
- Support client, GMP, and regulatory audits
- Identify and implement process improvements
- Increase site efficiency, quality, and throughput
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Native
- English – Business Fluent
Tools & Technologies
- LIMS
- PMP
- IPMA
Benefits
Flexible Working
- Flexible working hours
- Partial remote work
Competitive Pay
- Competitive compensation
- Equity
Learning & Development
- Training
- Certifications
Public Transport Subsidies
- Mobility opportunities
Diverse Work
- International projects
Modern Office
- Modern workplace
Modern Equipment
- Digital collaboration
Other Benefits
- Data integrity focus
- Attractive social benefits
- Diversity
- Inclusion
Sustainability Focus
- Sustainability
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Eurofins 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
Eurofins
Industry
Pharmaceuticals
Description
Das Unternehmen ist die führende Labor-Gruppe weltweit für Analyse- und Serviceleistungen in der Lebensmittel-, Pharma-, Umwelt- und Konsumgüterindustrie.
Not a perfect match?
- BLACKROLL AG
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Consultant SAP PS (Project System) & Project Management(m/w/x)
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Project Manager Operations(m/w/x)
Full-timeWith HomeofficeExperiencedRadolfzell am Bodenseefrom 80,000 / year