The AI Job Search Engine
BP Regulatory Affairs Manager(m/w/x)
Description
In this role, you will engage in a variety of tasks, including creating training materials and collaborating with teams and customers. Your focus will be on ensuring compliance with GMP guidelines and supporting quality initiatives across the organization.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in natural science, biotechnology, or comparable
- •Solid quality background with core GxP systems
- •Professional experience in quality or regulatory in pharma manufacturing
- •Professional experience with quality tools in pharmaceutical industry
- •Excellent communication skills in German and English
- •Accurate and detail-oriented mindset
- •Highly skilled in Microsoft Office applications
- •Passionated and motivating attitude
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Author and maintain internal guidance and training documentation
- •Collaborate with global functions, suppliers, and customers to share expertise
- •Review documents for alignment with GMP customer expectations
- •Provide targeted training sessions and participate in global presentations
- •Work closely with the Quality team to align on quality systems
- •Support colleagues in implementing requirements and translating them into solutions
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
More Vacation Days
- •Thirty vacation days per year
- •Company-regulated special leave days
Flexible Working
- •Flexible flextime framework
- •Working time account
- •Remote work across Germany
Retirement Plans
- •Employer-funded retirement plans
Company Bike
- •Job bike
Public Transport Subsidies
- •Public transport subsidies
Corporate Discounts
- •Corporate benefits
Learning & Development
- •Freely selectable training sessions
- •Participation in conferences
- •Access to learning platforms
Informal Culture
- •Diverse and open-minded work environment
- DASGIP Information and Process Technology GmbHFull-timeWith HomeofficeSeniorJülich
- DASGIP Information and Process Technology GmbH
Teamlead Product Support /Manager Technischer Support(m/w/x)
Full-timeWith HomeofficeManagementJülich - DASGIP Information and Process Technology GmbH
Quality Engineer(m/w/x)
Full-timeWith HomeofficeJuniorJülich - DASGIP Information and Process Technology GmbH
Supplier Quality Engineer(m/w/x)
Full-timeWith HomeofficeExperiencedJülich - AIXTRON SE
Senior Department Manager Industrial Quality(m/w/x)
Full-timeWith HomeofficeSeniorHerzogenrath
BP Regulatory Affairs Manager(m/w/x)
The AI Job Search Engine
Description
In this role, you will engage in a variety of tasks, including creating training materials and collaborating with teams and customers. Your focus will be on ensuring compliance with GMP guidelines and supporting quality initiatives across the organization.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in natural science, biotechnology, or comparable
- •Solid quality background with core GxP systems
- •Professional experience in quality or regulatory in pharma manufacturing
- •Professional experience with quality tools in pharmaceutical industry
- •Excellent communication skills in German and English
- •Accurate and detail-oriented mindset
- •Highly skilled in Microsoft Office applications
- •Passionated and motivating attitude
Education
Work Experience
approx. 1 - 4 years
Tasks
- •Author and maintain internal guidance and training documentation
- •Collaborate with global functions, suppliers, and customers to share expertise
- •Review documents for alignment with GMP customer expectations
- •Provide targeted training sessions and participate in global presentations
- •Work closely with the Quality team to align on quality systems
- •Support colleagues in implementing requirements and translating them into solutions
Tools & Technologies
Languages
German – Business Fluent
English – Business Fluent
Benefits
More Vacation Days
- •Thirty vacation days per year
- •Company-regulated special leave days
Flexible Working
- •Flexible flextime framework
- •Working time account
- •Remote work across Germany
Retirement Plans
- •Employer-funded retirement plans
Company Bike
- •Job bike
Public Transport Subsidies
- •Public transport subsidies
Corporate Discounts
- •Corporate benefits
Learning & Development
- •Freely selectable training sessions
- •Participation in conferences
- •Access to learning platforms
Informal Culture
- •Diverse and open-minded work environment
About the Company
DASGIP Information and Process Technology GmbH
Industry
Other
Description
Das Unternehmen bietet Gestaltungsspielraum in der Life-Science Branche und fördert ein wertschätzendes Arbeitsumfeld.
- DASGIP Information and Process Technology GmbH
Head of Global Bioprocess Service(m/w/x)
Full-timeWith HomeofficeSeniorJülich - DASGIP Information and Process Technology GmbH
Teamlead Product Support /Manager Technischer Support(m/w/x)
Full-timeWith HomeofficeManagementJülich - DASGIP Information and Process Technology GmbH
Quality Engineer(m/w/x)
Full-timeWith HomeofficeJuniorJülich - DASGIP Information and Process Technology GmbH
Supplier Quality Engineer(m/w/x)
Full-timeWith HomeofficeExperiencedJülich - AIXTRON SE
Senior Department Manager Industrial Quality(m/w/x)
Full-timeWith HomeofficeSeniorHerzogenrath