Gehaltsschätzung von jobs.ch:Melde dich an, um die Schätzung von jobs.ch zu sehen
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.
