Senior Expert R&D Developability and Formulation (m/f/d)
Octapharma Biopharmaceuticals GmbH
| Company | Octapharma Biopharmaceuticals GmbH |
| Category | Science & Research |
| Location | Heidelberg |
| Remote | — |
| Employment | Not stated |
| Level | Senior |
| Salary | Not stated by the employer |
| First seen | 2 Aug 2026 (the employer did not state a posting date) |
| Last verified | 10 Aug 2026 |
| Source | The employer's own careers page (company_site) |
Description
Your Profile:
• PhD or MSc in Pharmaceutical Sciences, Biochemistry, Chemistry, or related field, with proven industry experience in biologics formulation development
• Proven track record of advancing protein formulations through clinical development, ideally including late-stage or commercial products
• Strong expertise in parenteral formulations, including formulation design and excipient selection
• Experience in development subcutaneous drug product and lyophilization development is a strong plus
• Solid background in data-driven formulation development, applying DoE and QbD principles, with hands-on experience in biophysical and analytical characterization
• Sound understanding of ICH/GMP requirements and experience preparing CMC documentation for regulatory submissions (e.g., IND, CTA, BLA/MAA)
• Strong ability to drive scientific decisions, collaborate effectively in cross-functional teams (e.g., Analytics, Pilot Production, CMC/Regulatory stakeholders), and operate in a dynamic R&D environment
• Experience in advanced drug delivery approaches (e.g., oral delivery, sustained-release systems) is considered a plus
Your Tasks:
• Develop and define formulation strategies for protein drug candidates across all development stages, including stability assessment, excipient selection, and container-closure compatibility
• Lead formulation development programs, taking strong scientific ownership and coordinating external partners (e.g., CROs and CDMOs), while ensuring cross-functional alignment and data-driven decisions
• Plan, design, conduct, and critically review complex experimental studies, integrating advanced and risk-based approaches (e.g., DoE, QbD, stability modeling)
• Support scale-up and technology transfer to clinical manufacturing, ensuring robust translation into GMP production with internal teams and external partners
• Playing a leading role in CMC activities, including authoring, reviewing, and shaping documentation for regulatory submissions
• Drive innovation by leveraging scalable approaches, device and packaging solutions, and emerging technologies
• Mentor colleagues and contribute to scientific excellence, knowledge sharing, and continuous improvement
• Actively contribute to the department's scientific goals, innovation efforts, and cross-functional discussions, with a proactive and collaborative mindset