Senior Scientist Analytical Development
vor 2 Wochen
**The Position**:
Ready for your next professional challenge as a senior scientist in analytical development at Boehringer Ingelheim Animal Health? Become part of our team and become an expert in HPLC method development and in vitro dissolution for NCEs as we characterize our innovative pharmaceutical dosage forms using modern analytical methods. Your excellent specialist knowledge and commitment are the key to our success
**Tasks & responsibilities**:
- In your new role, you will develop, validate, and transfer relevant analytical methods including for in-vitro dissolution and ensure compliance with industrial GxP standards and VICH regulatory requirements.
- In addition, you will plan analytical activities using Quality by Design, interpret the results, draw the necessary scientific conclusions from them to derive the required specifications.
- Furthermore, you will also report and present your results internally, write scientific publications and show your results at international conferences.
- You will act independently as an analytical project representative in interdisciplinary development teams and successfully provide your analytical expertise up to market approval. Moreover, you will create global approval documents and interact with approval authorities worldwide.
- As a senior scientist, you will be responsible for the evaluation and implementation of innovative analytical technologies such as method development and in vitro dissolution to support the market approval of our new products with the latest scientific findings.
- Due to your experience in the GxP environment, you will take on responsibility as head of quality control and successfully represent the laboratory during official inspections and internal audits.
**Requirements**:
- PhD in the field of natural sciences with several years of industrial experience in product development, especially the analysis of various dosage forms such as tablets, suspensions, or solutions
- Solid specialist knowledge in a regulated environment (GMP, FDA, EU approval process)
- Extensive knowledge of analytical methods and equipment such as HPLC, in-vitro dissolution, GC, KF and FTIR
- Long term experience in creating analytical documents in English
- Advanced knowledge of statistical methods and process analysis
- Organizational talent as well as a high degree of initiative, flexibility, and the ability to work in a team
- Fluent in German and English
**Ready to contact us?**:
Recruitment process:
We reserve the right to take the posting offline beforehand. Applications up to January 19th, 2025 are guaranteed to be considered.
Step 2: Virtual meeting in the period from mid till end of January
Step 3: On-site interviews beginning till mid of February
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