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SIRE Life Sciences®

Open Application Assistant Scientist


SIRE Life Sciences®

Open Application Assistant Scientist

Location: Leiden, Netherlands

The company
It's a biotech company that focuses on the development, production and marketing of vaccines, recombinant proteins and antibodies to prevent and combat infectious and other diseases.

Job description
Based on formation plan and the needs within the QCD Labs organization, we are looking for a motivated Assistant Scientist who enjoys working in a multidisciplinary environment.

Responsibilities:
-Performing assays like: GPT and Control Cell Culturing of cells
-Ensuring that a high level of Quality is maintained in the department
-Accurate completion of documentation such as assay run sheets (ARS), laboratory notebooks and logbooks
-Actively participate in setting up documentation to ensure compliance
-Participate in continuous improvement projects that progresses the department in quality, EHS and efficiency gain
-Updating of test instructions for GMP assays.

Requirements:
-MLO or HLO degree
-Affinity with medical products
-Experience with quality and laboratory systems
-Experience with lab activities (e.g. cell culture) in a GMP environment or similar
-Good communication in English and Dutch (written and verbally)

Other Information:
For more information please apply via the button below.

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SIRE Life Sciences®

Job Description

The company
It's a biotech company that focuses on the development, production and marketing of vaccines, recombinant proteins and antibodies to prevent and combat infectious and other diseases.

Job description
Based on formation plan and the needs within the QCD Labs organization, we are looking for a motivated Assistant Scientist who enjoys working in a multidisciplinary environment.

Responsibilities:
-Performing assays like: GPT and Control Cell Culturing of cells
-Ensuring that a high level of Quality is maintained in the department
-Accurate completion of documentation such as assay run sheets (ARS), laboratory notebooks and logbooks
-Actively participate in setting up documentation to ensure compliance
-Participate in continuous improvement projects that progresses the department in quality, EHS and efficiency gain
-Updating of test instructions for GMP assays.

Requirements:
-MLO or HLO degree
-Affinity with medical products
-Experience with quality and laboratory systems
-Experience with lab activities (e.g. cell culture) in a GMP environment or similar
-Good communication in English and Dutch (written and verbally)

Other Information:
For more information please apply via the button below.

Additional Information

Last updated
Employment type
Full time
Contract type
Permanent
Number of vacancies
1
Min. experience
One year
Min. education
High School
Industry / category
Jobs in Laboratory / Biotechnology / Pharmacy