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, Support writing & reviewing analytical documents (e.g Analytical methods, Specificatios, 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, Proactively identifying scientific, GMP challenges, propose creative solutions and communicate key issues to the Analytical Project Leader or respective technical project team
Firmenprofil
Global pharma company
Arbeitsort
Basel
Arbeitsbeginn
Asap
Motivation
Are you looking to work in a global growth company where you can make a real difference? Then you are right with us!
Ausbildung
Master in analytical chemistry, equivalent or Jr. PhD
Salärrahmen
As per the industry
Erfahrungen
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)
Alter
Open
Sprachen
Deutsch: Von Vorteil
Englisch: Sehr gut
Spezielles
If you are interested then kindly send your resume to: v.agarwal@universal-job.ch
Vakanz-Nummer
P-13-6940
Global pharma company
Basel
Master in analytical chemistry, equivalent or Jr. PhD
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)
Chemie
P-13-6940
Temporär
v.agarwal@universal-job.ch