Posted in: Manufacturing and Production in Leiden | Posted: |
Job description Based on formation plan and the needs within the QCD Labs organization, we are looking for a motivated technician who enjoys working in a multidisciplinary environment. Main tasks of an Assistant Scientist are: - Taking part on all activities related to Release and Stability testing of cGMP TOX and clinical batches of Biopharmaceutical products: Vaccines. - Ensuring that a high level of Quality is maintained in the department. - Performing (Q)PCR assays like (auto)VPqPCR, QPA, HcDNA and IDPCR with a 'first time right attitude'. - Working precisely and on time data delivery with expected quality. (Perform assay, assay review and training). - 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. - Becoming assay responsible person for an assay performed within the team, including updating of test instructions for GMP assays. Minimum Qualifications - MBO / Bachelor (HBO) degree level with minimal of 2 years cGMP experience in the Pharmaceutical industry. - Working experience with cGMP is a plus. - Experience with biological assay. - You are motivated and have positive can-do attitude. - Previous experience working in a pharma/biotech will be a plus. - You have a good communication skills in English, written and spoken. - This is a fulltime position.