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Senior Expert (m/f/d) R&D Developability and Formulation
Octapharma Biopharmaceuticals GmbH
Heidelberg
Vollzeit
Flexible Arbeitszeiten
Jobticket
Kantine
Neu:
20.07.2026
Ref-Nr: 62794
Jetzt bewerben
Senior Expert (m/f/d) R&D Developability and Formulation
Jetzt bewerben
Jetzt bewerben
html Senior Expert (m/f/d) R&D Developability and Formulation
Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation.
Octapharma Biopharmaceuticals GmbH with more than 200 employees is a subsidiary of the Octapharma group founded in 1997 and successfully expanding. Our core business is the development of recombinant proteins produced in human cell lines for therapeutic use in humans. We strive for effective treatments with an improved tolerability and convenience for our patients.
Join us in shaping our vision to provide new health solutions advancing human life.
We are looking for a
Senior Expert (m/f/d) R&D Developability and Formulation
to join our state-of-the-art R&D Developability and Formulation group in Heidelberg. In this role, you will be responsible for developing robust drug product formulations for protein therapeutics from early development through clinical stages.
You will lead formulation strategy and development activities for injectable biologics, including liquid and lyophilized products, while supporting CMC and regulatory activities. Working closely with cross-functional teams and external partners, you will help advance our pipeline and contribute to next-generation drug product and delivery technologies.
Your main tasks and responsibilities
* 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 excellen...
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