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Quality Control Scientist
Eingestellt von Harvey Nash IT Recruitment Switzerland
Gesuchte Skills: Client
Projektbeschreibung
For our medical device client in Bern, we are looking for a Scientist for a contract role.
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
Would you like to apply for this job opportunity?
Please send me your updated CV: (see below) or feel free to contact me.
I am looking forward to hearing from you.
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
Would you like to apply for this job opportunity?
Please send me your updated CV: (see below) or feel free to contact me.
I am looking forward to hearing from you.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung