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Senior Expert R&D Developability and Formulation (m/f/d)

Octapharma Biopharmaceuticals GmbH
CompanyOctapharma Biopharmaceuticals GmbH
CategoryScience & Research
LocationHeidelberg
Remote
EmploymentNot stated
LevelSenior
SalaryNot stated by the employer
First seen2 Aug 2026 (the employer did not state a posting date)
Last verified10 Aug 2026
SourceThe employer's own careers page (company_site)
Applications are handled by the employer, not by us.Apply on the employer's 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