Assistant Scientist
Location: GermanySIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Pharmaceutical organization, based in .
They are an international company and their QC department is located in Leiden. Their QCD Release & Stability Department is responsible for cGMP testing of Release and Stability batches.
ROLE DESCRIPTION
A wide variety of Molecular Biological Assays as Analytical Assays are performed such as VP-QPCR, QPA, RP-HPLC, DCS, Sub-Visible Particle, WB, pH, Osmolality, HC DNA, HCP-ELISA and ID-PCR.
RESPONSIBILITIES
- 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 assays like: VP-QPCR, QPA, RP-HPLC, DCS, Sub-Visible Particle, WB, pH, Osmolality, HC DNA, HCP-ELISA and ID-PCR 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.
REQUIREMENTS
- 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 and or analytical assay.
- You have a good communication skills in English, written and spoken.
OTHER
- This is a fulltime position - 32 hours discussable
- Starting date: As soon as possible
- End date: February 2019 (+ potential extensions)
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Windimi Post.
