Jobdescription As part of the Global Drug Substance Development department, you will join a team of motivated scientists committed to developing and optimizing processes for the production of new biological therapeutics. The successful candidate will play a key role in designing and analyzing experimental studies related to the development of monoclonal antibodies (mAbs).
Key Responsibilities:
- Oversee process design deliverables, including Design of Experiments (DOE), experimental data analysis, reporting, and documentation for various programs.
- Report on the status of deliverables and study executions to the Drug Substance Development lead.
- Collaborate with cross-functional teams to optimize workflows and enhance process efficiency.
- Contribute to submissions by writing and reviewing documents in collaboration with regulatory dossier experts.
- Assist in the preparation of technical reports, presentations, and publications.
Qualifikationen Qualifications:
- PhD or Master's degree in a relevant scientific discipline (e.g., Biology, Biochemistry, Biotechnology).
- Experience in designing and analyzing experimental studies, preferably within the biopharmaceutical industry.
- Expertise in data analysis using DOE principles and scientific reporting.
- Strong attention to detail and excellent organizational skills.
- Ability to work collaboratively in a team-oriented environment.
- Effective communication skills, both written and verbal.
