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 field
* Minimum 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 required
* Good understanding of GMP required
* Experience with HPLC, CE or icIEF desirable
* Ideally experience with IT systems like LIMS and CDS
*Please note, only those with the right to work in Switzerland can apply!
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