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.
Job Description
SIRE 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.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Laboratory / Pharmacy / Biotech
