Job Description
Advancing medicine to save lives. Together. Thanks to many decades of experience and our passion for what we do, we make an essential contribution to the global availability of biopharmaceuticals, especially for patients with rare and serious diseases.
Rentschler Biopharma SE is a leading contract development and manufacturing organization (CDMO) focused exclusively on client projects. We offer customized full-service solutions for bioprocess development and the production of complex biopharmaceuticals. As a German family-owned company with an international footprint and global reach, we combine experts, expertise and years of experience to develop best-in-class solutions - together with our clients.
Rentschler Biopharma has approximately 1,400 employees and is headquartered in Laupheim, Germany, with a site in Milford, MA, USA. In 2024, we joined the United Nations Global Compact, underlining our commitment to sustainability.
As an independent family-owned company, we live by the motto: Many hands, many minds - ONE TEAM! Open, respectful cooperation characterizes our working environment, where quality awareness, diligence and responsibility are our top priorities. With all the diversity of our talents in the Rentschler team, we pursue one vision together: advancing medicine to save lives.
Duties and Responsibilities - Analyze raw process and analytical data related to upstream process development
- Independently prepare reports and publications based on raw data from process development and production
- Review reports from process development and production for accuracy and completeness
- Actively participate in internal projects, such as the standardization of documents
- Assist in the preparation of posters and presentations for scientific communication
- Participate in interdisciplinary meetings and ensure alignment between teams on documentation goals
- Support the creation and review of general technical documents, including policies, SOPs, and templates
- Prepare and review cGMP documents, such as protocols, reports, batch records
- Provide guidance to team members on scientific writing best practices
Qualifications - Master's degree or relevant experience in biotechnology, biochemistry, or a comparable scientific/technical field
- 5+ years of applicable scientific writing experience in a biopharmaceutical environment
- Preferably demonstrates a track record of peer-reviewed publications as the lead author
- Advanced knowledge in biotechnical manufacturing processes and USP/DSP development
- Strong understanding of biostatistics and the ability to apply statistical methods to process development
- Proficiency in Microsoft Office Suite (Word, Excel, PowerPoint); experience with additional software/tools related to scientific writing and data analysis is a plus
- Excellent written and verbal communication skills, with demonstrated ability to depict and present complex scientific data in a clear and comprehensible manner
- Detail oriented regarding grammar, orthography, scientific precision, layout, and design
- Basic knowledge in project management
- Self-motivated, accountable, and highly organized, with excellent time-management skills
- Ability to work independently and collaboratively in a cross-functional team environment
Working Conditions - Normal office working conditions: computer, phone, files, copier
- Will interact with other people
- Pace may be fast and job completion demands may be high
Physical Requirements Rentschler
Job Tags
Contract work,