For our client we are looking for a highly motivated Analytical Expert in the field of small molecules. You will be responsible for: - Planning, interpreting and reporting results of scientific experiments for timely supply of drug substances (DS) and drug products (DP) - Performing raw data checks for externalized activities - Writing & reviewing analytical documents (e.g Analytical methods, Specifications, Validation reports, Stability reports, Batch records for stability and release testing) and aligning the corresponding activities within a global project team - Managing interactions with internal and external stakeholders, including outsourced activities to CROs by providing scientific and technical guidance whenever necessary
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Global Pharma Company.
If you are interested then kindly send your resume to: firstname.lastname@example.org
- At least 4 years’ experience in the pharmaceutical industry with a track record in GMP activities for development or marketed products - Profound expertise in analytical raw data documentation, documentation writing (Stability Report, Validation etc) - Broad scientific knowledge in chemistry, pharmaceutical or analytical sciences, ability to perform in a highly dynamic environment - Advanced knowledge of laboratory and/or technical tools (e.g. HPLC, LC-MS, Quality management systems, statistical evaluation tools ...) - Good knowledge of commonly used software and computer tools - Good scientific/technical writing skills - Experience is Inhaled dosage form is a plus
PhD or minimum Master in analytical chemistry or equivalent
English : Very good