Location
Heidelberg | Germany
Job description
ProtaGene is a leading global CRO partner for the biopharmaceutical, cell and gene therapy industries. From research to product commercialization, we provide the most advanced, integrated and complete protein and gene analytical capabilities and packages for biologic therapeutics and cell and gene therapy platforms. Our long-standing analytical leadership in protein-based therapeutics stems from the merger of Protagen Protein Services in Europe and BioAnalytix in the US. In 2021, our portfolio was expanded to include GeneWerk's unique capabilities in vector safety, integration site analysis and bioinformatics, creating ProtaGene. Our combined protein and gene-based analysis platforms make the company the leading provider of analytical services in the fields of biopharmaceutical, cell and gene therapy development. The company operates four sites in Europe and North America and collaborates on advanced therapeutic platforms with leading biopharmaceutical and gene therapy companies worldwide.
Scientist (m/f/d)
Heidelberg
Aufgaben:
- Analyzing laboratory data for customer projects and managing and implementing customer projects.
- Evaluate analytical results and contribute to the preparation of reports.
- Responsibility for the prompt and accurate collection of raw data according to the controlled documents and in accordance with the regulations/principles of GCP/GLP/GCLP and for the quality of these data.
- Execution and coordination of trial and project planning, research of literature regarding existing strategies and evaluation of their applicability.
- Forming working hypotheses on the functional relationship between the processes.
- Interpretation of the results, verification/falsification of the hypotheses, documentation.
- Analyzing and documenting the experimental data and preparing e.g. graphics, PowerPoint presentations, posters, publications if necessary.
- Presentation of the results; e.g. presentations at research meetings.
- Participation in the preparation of controlled documents.
Qualifikationsprofil:
- Successfully completed scientific and technical Master's degree in the life sciences (e.g. biology / biochemistry / molecular medicine) or comparable qualification.
- Sound knowledge of the regulations/principles according to GCP/GLP/GCLP desirable.
- Scientific background in gene therapy desirable.
- Basic knowledge in Bioinformatics for NGS data analysis are of advantage.
- Willingness to carry out work according to GCP/GLP/GCLP guidelines and to support the development/maintenance of the QM system.
- The ability to work in a team and to work very accurately and precisely is essential.
- High level of initiative and the ability to work independently and goal orientated in a fast paced, dynamic environment to quality management standards.
- You are characterized by a very careful and precise way of working.
- You enjoy and are interested in complex analytical issues.
- Sound IT skills as well as very good English skills for working in an international team and with international customers.
- Diligence, reliability, and organizational talent round off your profile.
Benefits:
- Responsible and varied tasks in a motivating working environment.
- A permanent position in a dynamically growing international life science group of companies with over 200 employees.
- Optimal familiarization and training opportunities as well as individual development options.
- Appreciation, openness, and respect as well as a lively feedback culture.
- Flat hierarchies, short decision-making processes and flexibility.
- Comprehensive health management.
- Job Ticket.
- Regular company and team events.
Job tags
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