Your tasks
* Assessment and allocation of available laboratory capacities within Formulation Development and Analytical Development teams aligned with project timelines and organizational goals
* Securing the timely availability of all required materials necessary for conducting compatibility studies in alignment with procurement responsible
* Revision of test plans for compatibility studies
* Investigation out of specification results
* Writing analytical reports & presenting analytical data
* Review and assessment of study reports, ensuring they meet internal and external regulatory requirements
* Maintain up-to-date knowledge of international standards (EU-GMP, US-cGMP, ISO 9001, 21 CFR 4, 21 CFR 820) and internal guidelines (SOPs and cWIs)
Our expectations
* University degree in Chemistry, Technical Chemistry or Biochemistry
* Strong skills in understanding and interpretation of analytical data of compounded parenteral formulations with a specific focus on particle characterization (Mastersizer, Accusizer)
* Strong organizational, planning, and communication skills
* Proficiency in MS Office applications, with excellent command of Word, Excel, and Power Point
* Exceptional written and verbal German and English skills, enabling effective collaboration with global teams
* Strong interpersonal skills with the ability to work collaboratively in a team environment
We offer
* International challenges in a dynamic corporate environment
* Training opportunities and personal development within the company
* Corporate social events
* Attractive performance-related salary package (annual gross salary € 63.000,-; overpayment dependent on occupational skills and experience)
We are caring for our employees
* Reliable employer
* Strong global growth
* International career opportunities
* Comprehensive education and training
* Homeoffice
* Jobticket
* Active health promotion
* Free parking space
* Bikeleasing
* Canteen
* Joint company events
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