Bioanalytical Junior Specialist
Duchnice
Boost your career with us
Polpharma Biologics is a state-of-the-art biological R&D and manufacturing facility, one of the most modern in Europe. We have a fantastic, international team of experienced experts and dynamic young scientists with common goals and values. Biotechnology is our passion.
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Together we develop medicines, offering a new hope to patients suffering from serious diseases. We create a passionate and friendly workplace environment. Join us!
Your responsibilities
- Conducting research related to the development of new and modification of existing analytical methods for control of active substances (pharmacologically active biological particles) and biotechnological medicinal products.
- Conducting analytical method qualification and method transfer to Quality Control section or other external company.
- Performing tests of analytical control of the substances and the drug form during its development and during technical batch runs.
- Analyzing and interpreting the results of research carried out during development and during technical batch runs.
- Keeping records of the carried out research, transfer and/or qualification/validation of methods in accordance with existing standard operating procedures and the principles.
- Developing standard operating procedures and instructions and conducting the training on them.
- Perform maintenance, calibration and qualification of physicochemical equipment in accordance with the instructions and procedures.
- Reviewing the specialist literature in order to select the appropriate analytical control methods for new substances and biotechnology drug form.
- Controlling the usage and preparation of purchasing requests for direct and supporting materials as well as substances and reagents used during the research.
- Supporting activities related to the creation of Analytical Development laboratory with the use of good laboratory practices as well as organizational and safety standards
- Writing User Specification Requirements (URS) and participation in the equipment purchase process
- Supporting the work of team members in the preparation of documents such as SOP, protocols and reports, and other laboratory tasks.
- Providing technical and scientific support for laboratory analytical methods.
- Carrying out activities aimed at ensuring the functioning of the laboratory in accordance with the principles of health and safety, hygiene, environmental protection and 6S.
If you have
- Higher education in the field of: biotechnology, biology, biochemistry or related.Min.0-2 years of experience in laboratory work (analytical or quality control laboratory) in biotechnological or pharmaceutical company
- Knowledge of analytical techniques such as: ELISA, Cell culture, Microplate reader, microscope, FACS, Cell banking, Immunoassays, PLA software.
- Knowledge of topics related to GxP
- Experience in writing procedures, protocols and reports.
- The ability to think creatively and the ability to collaborate with others to solve technical problems.
- Good organization of work and time
- Knowledge of MS Office
- Very good command of spoken and written English.