CMC/Formulation Scientist/Senior Scientist – Inhalation
Job in
Germany, Pike County, Ohio, USA
Listed on 2026-03-06
Listing for:
OINDPnews
Full Time
position Listed on 2026-03-06
Job specializations:
-
Pharmaceutical
Pharmaceutical Science/ Research -
Research/Development
Research Scientist, Pharmaceutical Science/ Research
Job Description & How to Apply Below
Location: Germany
CMC/Formulation Scientist / Senior Scientist – Inhalation
Posted on OINDPnews on August 23, 2022
Company: Sandoz
Within our Pharmaceutical Development department, you will be a CMC /Formulation Expert – Scientist / Senior Scientist – (d/f/m) responsible for planning, conducting and evaluating scientific studies in the pharmaceutical development of inhaled drugs. You will function as a core member of the technical project team. Depending on the level and area of expertise, the job title and objectives may vary.
Yourkey responsibilities
Your responsibilities include, but are not limited to:
- Planning, execution and evaluation of scientific studies in the context of the pharmaceutical development of inhaled drugs
- Act as core member of the technical project team
- Coordination of development work with internal and external development partners
- Ensure compliance with Regulatory and Quality requirements for technical product development in accordance with internal, national and international guidelines (GMP, ICH, etc.) in order to guarantee successful approval of the development project
- Assess and consolidate with the project leader and other key stakeholders all resource needs and timelines for assigned projects
- Use the possibilities offered by modern formulation, process and analytical technologies to progress projects in a timely manner
- PhD (preferred), MS, or BS in Chemistry, Pharmacy, or related field.
- Experience in the development or production of pharmaceutical products, preferably in the development of inhaled drugs
- Good understanding of the material characteristics which influence and optimize drug product performance
- Confidence in the GMP environment and understand the most important national and international guidelines
- Fluency in spoken and written English and ideally in German
- Presentation skills to communicate effectively to peers and senior management
- Scientific writing skills to complete Regulatory submission documentation
- Team player, independent and results-oriented
Position Requirements
10+ Years
work experience
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