• An agile career and a dynamic work culture
• An inclusive and ethical workplace
• Compensation programs that recognize high performance
• In addition to competitive salaries, you'll find a wide range of lifestyle, family, and leisure benefits. Depending on the location, these benefits may include family allowances, childcare support, discounts at local businesses and attractions, travel allowances, and subsidized meals.

Your tasks:

• Independent application of biochemical analysis methods with a focus on ELISA, gel electrophoresis and rDNA analysis.
• Collaboration in method development, implementation, transfer and validation, as well as in data evaluation and solving analytical problems – especially in the field of cell-based assays.
• Planning, coordination and execution of release tests as well as technical support for analytical and technical issues in the GMP environment.
• Independent handling of deviations, change requests and investigations within the framework of regulatory requirements.
• Evaluation and interpretation of analytical data as well as preparation of scientific reports and presentations.
• Drafting, reviewing and approving quality-relevant documents to ensure compliance with legal and internal requirements.
• Independent execution of assigned tasks within the framework of studies and projects with a focus on quality, safety and adherence to deadlines.

Your requirements profile:

• Completed degree in natural sciences (BSc or higher) in biology, biochemistry, chemistry or a related field
• Ideally, initial professional experience in quality control or analysis of biopharmaceuticals, preferably in a regulated GMP environment.
• Independent, structured and solution-oriented work style
• Taking on responsibility and actively contributing professional expertise to the team
• High quality awareness, initiative and commitment
• Excellent German skills (spoken and written) and good English skills