The AI Job Search Engine
Scientific Writer(m/w/x)
Description
In this role, you will transform complex biopharmaceutical data into clear, structured documentation, ensuring compliance and transparency throughout the development and manufacturing processes. Your responsibilities include analyzing data, drafting reports, and maintaining high quality standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in a scientific discipline
- •Peer-reviewed publications as first author
- •Knowledge of biotechnological development processes (USP/DSP)
- •Excellent English skills (written and spoken)
- •Solid understanding of DoE and biostatistics
- •Basic project management knowledge
- •Ability to present complex data clearly and logically
- •Strong attention to detail in language, scientific accuracy, and formatting
- •Proficiency in MS Office and JMP
- •Experience in preparing regulatory documents is advantageous
- •Skills in visualizing scientific content is a plus
- •Affinity for interdisciplinary collaboration
Education
Tasks
- •Analyze raw data from process development
- •Prepare and review reports from Process Science and Manufacturing Science and Technology
- •Draft and review protocols, policies, and overarching SOPs
- •Write clear, structured reports for early, late-stage, and commercial process development
- •Present complex data in an understandable and scientifically accurate way for stakeholders
- •Ensure high standards in grammar, scientific precision, layout, and design
- •Contribute to document harmonization and standardization projects
Tools & Technologies
Languages
English – Business Fluent
Benefits
Purpose-Driven Work
- •Meaningful work
Informal Culture
- •Inspiring work atmosphere
Learning & Development
- •Individual development opportunities
- •Comprehensive onboarding program
Flexible Working
- •Flexible work arrangements
More Vacation Days
- •30 vacation days
- •Special leave days
Free or Subsidized Food
- •Cafeteria with vegetarian/vegan options
Healthcare & Fitness
- •Corporate health management
- •Company doctor
Team Events
- •Team and company events
Corporate Discounts
- •Variety of employee discounts
Public Transport Subsidies
- •Discounts on job ticket
Additional Allowances
- •Financial relocation support
Parking & Commuter Benefits
- •Free parking
- Rentschler Biopharma SEFull-timeWith HomeofficeEntry LevelLaupheim
- Rentschler Biopharma SE
Prozessingenieur / Scientist Downstream Entwicklung(m/w/x)
Full-timeWith HomeofficeNot specifiedLaupheim - Rentschler Biopharma SE
Process Manager - MSAT - DSP(m/w/x)
Full-timeWith HomeofficeExperiencedLaupheim - Rentschler Biopharma SE
Pharmazeutischer Operator USP Produktion(m/w/x)
Full-timeWith HomeofficeNot specifiedLaupheim - Rentschler Biopharma SE
Prozessingenieur Downstream Production(m/w/x)
Full-timeWith HomeofficeExperiencedLaupheim
Scientific Writer(m/w/x)
The AI Job Search Engine
Description
In this role, you will transform complex biopharmaceutical data into clear, structured documentation, ensuring compliance and transparency throughout the development and manufacturing processes. Your responsibilities include analyzing data, drafting reports, and maintaining high quality standards.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Degree in a scientific discipline
- •Peer-reviewed publications as first author
- •Knowledge of biotechnological development processes (USP/DSP)
- •Excellent English skills (written and spoken)
- •Solid understanding of DoE and biostatistics
- •Basic project management knowledge
- •Ability to present complex data clearly and logically
- •Strong attention to detail in language, scientific accuracy, and formatting
- •Proficiency in MS Office and JMP
- •Experience in preparing regulatory documents is advantageous
- •Skills in visualizing scientific content is a plus
- •Affinity for interdisciplinary collaboration
Education
Tasks
- •Analyze raw data from process development
- •Prepare and review reports from Process Science and Manufacturing Science and Technology
- •Draft and review protocols, policies, and overarching SOPs
- •Write clear, structured reports for early, late-stage, and commercial process development
- •Present complex data in an understandable and scientifically accurate way for stakeholders
- •Ensure high standards in grammar, scientific precision, layout, and design
- •Contribute to document harmonization and standardization projects
Tools & Technologies
Languages
English – Business Fluent
Benefits
Purpose-Driven Work
- •Meaningful work
Informal Culture
- •Inspiring work atmosphere
Learning & Development
- •Individual development opportunities
- •Comprehensive onboarding program
Flexible Working
- •Flexible work arrangements
More Vacation Days
- •30 vacation days
- •Special leave days
Free or Subsidized Food
- •Cafeteria with vegetarian/vegan options
Healthcare & Fitness
- •Corporate health management
- •Company doctor
Team Events
- •Team and company events
Corporate Discounts
- •Variety of employee discounts
Public Transport Subsidies
- •Discounts on job ticket
Additional Allowances
- •Financial relocation support
Parking & Commuter Benefits
- •Free parking
About the Company
Rentschler Biopharma SE
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein führender Auftragsentwicklungs- und Herstellungsbetrieb (CDMO), der sich auf biopharmazeutische Lösungen spezialisiert hat.
- Rentschler Biopharma SE
Product Expert / Analytical Process Manager(m/w/x)
Full-timeWith HomeofficeEntry LevelLaupheim - Rentschler Biopharma SE
Prozessingenieur / Scientist Downstream Entwicklung(m/w/x)
Full-timeWith HomeofficeNot specifiedLaupheim - Rentschler Biopharma SE
Process Manager - MSAT - DSP(m/w/x)
Full-timeWith HomeofficeExperiencedLaupheim - Rentschler Biopharma SE
Pharmazeutischer Operator USP Produktion(m/w/x)
Full-timeWith HomeofficeNot specifiedLaupheim - Rentschler Biopharma SE
Prozessingenieur Downstream Production(m/w/x)
Full-timeWith HomeofficeExperiencedLaupheim