We are currently searching for a Scientist for one of our clients, an international biopharmaceutical company in Visp.
Responsibilities :
- Implementation, optimization, transfer and validation of analytical methods, with focus on HPLC, CE and icIEF
- Planning and implementation of release and stability analytics
- Responsibility for all HPLC project related tasks and representation of HPLC team in the project team for the assigned projects
- Processing of investigations, change requests and deviations under cGMP
- Extraction and evaluation of analytical data, preparation of reports and presentations
- Preparation, review and approval of documents to ensure compliance with regulatory guidelines
- Expertise in analytical and technical issues for the assigned projects
Key requirements :
Bachelor, Master or PhD in chemistry, biochemistry, biology or related fieldMinimum 5 years of relevant experience in pharma industry with Bachelor degree, minimum 3 years of relevant experience in pharma industry with Master degree, PhD no experience in pharma industry requiredGood understanding of GMP requiredExperience with HPLC, CE or icIEF desirableIdeally experience with IT systems like LIMS and CDSFluent in EnglishFor further information about this position, please apply with your CV
Please note, only those with the right to work in Switzerland can apply!