• Contract
  • Hessen
  • Recruiter: Ashwini Shirvaikar

The Life Science Career Network

CTC are specialised industry experts who can help companies source the best talent and provide reliable HR and consulting services, support varied candidates in finding promising career opportunities and offer the latest in skill development training programmes.

Our client is a global biopharmaceutical company and leader in manufacturing plasma-derived and recombinant therapeutic products in more than 100 countries. The company is committed to treating rare and serious diseases and improving the quality of life of patients around the world.

Scientist (m/w/d)

For the site located in Marburg, Germany, we are looking for a  Scientist to step in a contract role for a 12 months on a temporary basis (Arbeitnehmerüberlassung) .

Key Responsibilities:

  • Preparation of risk analyses regarding pathogen safety on deviations, process changes and pharmacovigilance requests
  • Preparation of manuscripts/opinions regarding pathogen safety for submission to regulatory authorities
  • Preparation of SOPs
  • Development of experimental study designs in coordination with the supervisor
  • Planning and execution of experiments including data analysis and communication of results usually to the manager or, if necessary, to the project team in the form of a report or a presentation to the project team in the form of a report or presentation
  • Evaluation of the results of the experiments and derivation of recommendations for action
  • Operation of complex equipment, program scripting and processing and preparation of raw data from analyses
  • Contributions to congresses, preparation of publication drafts
  • Procurement, collection, preparation and distribution of samples also in coordination with other areas, e.g. Coordination of research projects as Project Scientific Coordinator
  • Technical contact as expert for specific processes and equipment
  • Contacting and obtaining information from external suppliers and collaboration partners
  • Creation and maintenance of records in internal documentation systems
  • Support in the preparation of written contributions to regulatory documents (e.g., applications for marketing authorization, etc.)
  • Preparation and revision of technical documents, including work instructions, test or process protocols and reports (relevant for submission)
  • Technical preparation of decision bases for procurement of new equipment and systems
  • Maintenance of laboratory and equipment according to required quality standards (e.g. APS, GLP or GMP
  • Perform maintenance/calibration work or coordinate repair work on scientific equipment in collaboration with internal or external service provider
  • Plan and perform equipment qualification
  • Coordinate the availability of materials, solutions and reagents
  • Control and maintain biological systems (e.g., cell cultures)

Qualifications & Experience:

·        Natural science studies (preferably biochemistry but also biology, biotechnology and related studies)

·        Must Have – Knowledge in biochemistry, virology, immunology

·        Nice to have – Doctorate, work experience in the pharmaceutical industry (preferably biotherapeutics, plasma proteins)

·        Profile for office staff, no laboratory activities

·        Remote work 3 days per week

Would you like to learn more about CTC and the opportunity outlined? Please, get in contact with us: you may either use the 'apply now' button, or write an email to us, or reach out to us on the phone