- Global Pharmaceutical Organization based in Northern Suburbs
- Seeking Experienced R&D Scientist to join their team on a 12-month contract basis.
- This is a full-time contract position
- Monday - Friday but may be required to attend global calls so will need to be available some evenings.
Reporting to the R&D Manager this role will incorporate both laboratory-based work as well as documentation/report writing.
Your responsibilities include but are not limited to:
- Perform laboratory studies using viruses (including human pathogens) to support pathogen safety assessments of manufacturing processes
- Create templates for study and regulatory documentation (R&D study reports, regulatory section for CMC dossier)
- Generation of technical reports for use in regulatory submissions based on templates
- Contribute to the development and validation of scale-down models
- Supporting manufacturing in deviations and change control
- Contribute to the research and development of new viral clearance strategies
- Analyse and interpret experimental data
- Ensure compliance to GLP and GMP (where applicable)
- Tertiary qualification in an appropriate scientific discipline, including Biochemistry, Microbiology or Biomedical Science (PhD or Masters preferred)
- Proficiency in German language (highly desirable)
- Background in virology (highly desirable)
- Experience in data analysis, experimental design, and ability to develop detailed understanding of scientific rationale
- Understanding and experience working under GLP and/or GMP (required)
- Good problem solving and analytical skills with attention to detail
- Strong verbal and written communication skills
- Good team working skills
If you think this could be the role for you then please apply now! Please send us a cover letter AND a detailed resume in WORD format (PDFs can be corrupted / not processed).
Or, if you have any questions, please contact Deborah or Sarah on 03 9040 1***.
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