Senior Analytical Manager Compatibility Studies (m/f/d)

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)