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Quality Control Scientist
Eingestellt von Harvey Nash IT Recruitment Switzerland
Projektbeschreibung
Role: Quality Control Scientist Analyst
Place of work: Bern
Beginning of employment: 01.09.2016
End of employment: 31.05.2017
Workload: 100%/40 hours
In this position you are responsible for on time implementation of new analytical methods (eg RP-, SE-, and Ion chromatography, ELISA, Western Blot and gel based techniques) within the QC laboratories and you act as interface with other departments and functions according to business requirements. As a scientific expert in Quality Control department you are responsible for planning, coordination and evaluation of related project work and you are extensively involved in the transfer and validation of analytical methods. You are also familiar with equipment qualification and CSV activities. You will profit from your scientific background and analytical mindset for reporting, analysis and interpretation of obtained results, including writing scientifically sound technical documents, instructions, protocols and reports. In addition, you are experienced to work in a GMP regulated environment and your easy-going nature will allow you to deliver to agreed timelines. Your team spirit will allow you to integrate into the team and ideally you have experience in supervising the work of laboratory technicians.
Tasks:
" Implementation of new analytical methods including method validation, equipment qualification and CSV activities
" Interface with the other QC teams and other departments and functions
" Writing scientifically sound technical documents, instructions, protocols and reports
" Provide laboratory technicians with training and supervise problem solving and execution of laboratory investigation
" Management and execution of analytical methods life cycle activities (for IPC, release, stability, monitoring testing)
" Take over deputy activities for the QC Analytics Team Leader
Qualifications
" BSc, Master or PhD in Chemistry, Biochemistry or a related field with an analytical background and a minimum of 5 years of professional experience in pharma, biotech or vaccine industry
" Extensive experience in analytical method transfer and method validation, CSV and equipment qualification
" In-depth knowledge/hands-on experience with an extensive range of analytical technologies and bioassays (HPLC, IC, GC, IEF, SDS-PAGE, ELISA)
" Familiar with all aspects of compendial testing and related industry guidelines
" Excellent knowledge and experience in GMP
" Demonstrate innovative spirit, strong interpersonal and leadership skills and project management
" Ability to work in an dynamic environment according to tight and challenging timelines
" Flexible team player with the ability and willingness to deputies for the team leader
" Business fluent in German and English
Place of work: Bern
Beginning of employment: 01.09.2016
End of employment: 31.05.2017
Workload: 100%/40 hours
In this position you are responsible for on time implementation of new analytical methods (eg RP-, SE-, and Ion chromatography, ELISA, Western Blot and gel based techniques) within the QC laboratories and you act as interface with other departments and functions according to business requirements. As a scientific expert in Quality Control department you are responsible for planning, coordination and evaluation of related project work and you are extensively involved in the transfer and validation of analytical methods. You are also familiar with equipment qualification and CSV activities. You will profit from your scientific background and analytical mindset for reporting, analysis and interpretation of obtained results, including writing scientifically sound technical documents, instructions, protocols and reports. In addition, you are experienced to work in a GMP regulated environment and your easy-going nature will allow you to deliver to agreed timelines. Your team spirit will allow you to integrate into the team and ideally you have experience in supervising the work of laboratory technicians.
Tasks:
" Implementation of new analytical methods including method validation, equipment qualification and CSV activities
" Interface with the other QC teams and other departments and functions
" Writing scientifically sound technical documents, instructions, protocols and reports
" Provide laboratory technicians with training and supervise problem solving and execution of laboratory investigation
" Management and execution of analytical methods life cycle activities (for IPC, release, stability, monitoring testing)
" Take over deputy activities for the QC Analytics Team Leader
Qualifications
" BSc, Master or PhD in Chemistry, Biochemistry or a related field with an analytical background and a minimum of 5 years of professional experience in pharma, biotech or vaccine industry
" Extensive experience in analytical method transfer and method validation, CSV and equipment qualification
" In-depth knowledge/hands-on experience with an extensive range of analytical technologies and bioassays (HPLC, IC, GC, IEF, SDS-PAGE, ELISA)
" Familiar with all aspects of compendial testing and related industry guidelines
" Excellent knowledge and experience in GMP
" Demonstrate innovative spirit, strong interpersonal and leadership skills and project management
" Ability to work in an dynamic environment according to tight and challenging timelines
" Flexible team player with the ability and willingness to deputies for the team leader
" Business fluent in German and English
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Sonstiges