q.beyond AG
Consultant SAP Manufacturing(m/w/x)
Full-timeWith HomeofficeExperienced
Oberhausen, Hamburg, Leipzig, Köln, Darmstadt, Ulm, Augsburg
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MIMiltenyi Biotec
Manufacturing Expert Software(m/w/x)
Bergisch Gladbach
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Designing, configuring, and validating MES workflows for pharmaceutical manufacturing. Experience with MES and regulated environments required. International teams, corporate sports, and health provision.
Requirements
- Degree in Automation, Industrial IT, Engineering, Pharmaceutical Manufacturing, or related technical field
- Relevant experience with Manufacturing Execution Systems (MES)
- Experience in pharmaceutical or regulated manufacturing
- Solid understanding of Computerized System Validation (CSV) is an advantage
- Strong analytical mindset
- High accuracy and attention to detail
- Configuring, testing, documenting, and delivering MES solutions
- Ability to thrive in dynamic environments
- Strong task prioritization skills
- Strong project management skills
- Excellent verbal communication skills
- Excellent written communication skills
- Technical documentation skills
- English language mandatory
- German language is a plus
Tasks
- Design, configure, test, validate, and maintain MES workflows
- Ensure compliant and efficient manufacturing execution
- Integrate MES workflows with ERP systems and manufacturing equipment
- Support end-to-end digital production processes
- Create and maintain technical documentation
- Develop SOPs, user manuals, and validation test cases
- Ensure cGMP and data integrity compliance
- Collaborate with Manufacturing, QA, QC, IT, and external partners
- Translate operational and regulatory requirements into MES solutions
- Provide user training and on-site technical support
- Communicate regularly with internal stakeholders
- Report to the MES System Owner
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- Manufacturing Execution Systems (MES)
Benefits
Informal Culture
- International teams
- Cross-border intercultural communication
Healthcare & Fitness
- Corporate sports activities
- Health provision
Learning & Development
- Inhouse Training Academy
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Miltenyi Biotec 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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MIMiltenyi Biotec
Manufacturing Expert Software(m/w/x)
Bergisch Gladbach
Full-timeWith Home OfficeExperienced
Nejo AI Summary
Designing, configuring, and validating MES workflows for pharmaceutical manufacturing. Experience with MES and regulated environments required. International teams, corporate sports, and health provision.
Requirements
- Degree in Automation, Industrial IT, Engineering, Pharmaceutical Manufacturing, or related technical field
- Relevant experience with Manufacturing Execution Systems (MES)
- Experience in pharmaceutical or regulated manufacturing
- Solid understanding of Computerized System Validation (CSV) is an advantage
- Strong analytical mindset
- High accuracy and attention to detail
- Configuring, testing, documenting, and delivering MES solutions
- Ability to thrive in dynamic environments
- Strong task prioritization skills
- Strong project management skills
- Excellent verbal communication skills
- Excellent written communication skills
- Technical documentation skills
- English language mandatory
- German language is a plus
Tasks
- Design, configure, test, validate, and maintain MES workflows
- Ensure compliant and efficient manufacturing execution
- Integrate MES workflows with ERP systems and manufacturing equipment
- Support end-to-end digital production processes
- Create and maintain technical documentation
- Develop SOPs, user manuals, and validation test cases
- Ensure cGMP and data integrity compliance
- Collaborate with Manufacturing, QA, QC, IT, and external partners
- Translate operational and regulatory requirements into MES solutions
- Provide user training and on-site technical support
- Communicate regularly with internal stakeholders
- Report to the MES System Owner
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degree
Languages
- English – Native
- German – Basic
Tools & Technologies
- Manufacturing Execution Systems (MES)
Benefits
Informal Culture
- International teams
- Cross-border intercultural communication
Healthcare & Fitness
- Corporate sports activities
- Health provision
Learning & Development
- Inhouse Training Academy
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Miltenyi Biotec 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
Miltenyi Biotec
Industry
Healthcare
Description
Das Unternehmen entwickelt einzigartige Lösungen für die biomedizinische Spitzenforschung sowie neuartige Zell- und Gentherapien.
Not a perfect match?
- q.beyond AG
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Full-time/Part-timeWith HomeofficeExperiencedBerlin, Hamburg, Köln, Stuttgart, Dortmund, Dresden, Bielefeld, Heidelberg, Göttingen, Pforzheim - Bayer
Pharmakant:in / Chemikant:in in der pharmazeutischen Produktion(m/w/x)
Full-timeTemporary contractWith HomeofficeJuniorLeverkusen