Scientist, Flow Cytometry

Alliance Pharma Pty Ltd

  • Comply with laboratory health and safety standards.
  • Knowledge and understanding of regulatory requirements; GLP, GCP, 21CFR Part 11
  • Ability to follow standard operational procedures, apply established principles to maintain services in accordance with NATA/ISO accreditation requirements.
  • Maintain strong knowledge of immunology principles.
  • Operation and maintenance of flow cytometers.
  • Participate in research, design and development of 10+ color flow cytometry analytical methods, including troubleshooting.
  • Analyze samples following validated analytical methods including data review and interpretation using FCS express.
  • Maintain accurate and detailed experimental records, review data, and contribute to technical reports.
  • Perform quality control checks
  • Collaborate closely with project teams, study directors/PI, and QA to ensure timely and high-quality study delivery.
  • Train and mentor junior level scientists.
  • Drafting/reviewing SOPs, methods and reports.
  • Collaborate across teams, departments, and sites.
  • Participate in ongoing laboratory and regulatory training.
  • Assists with any additional tasks assigned by management.
  • Embrace and promote laboratory character
  • Adaptable to varying timelines and responsibilities.
  • Bachelor’s degree or higher with at least 3 years of relevant work experience, or an equivalent combination of education, training, and experience as deemed appropriate by management.
  • At least 2 years of experience in flow data analysis and interpretation.
  • Experience using FCS express is desirable.
  • Detail oriented and responsible.
  • Ability to work effectively in a team as well as work independently.
  • Strong collaboration, time management, and organizational skills.
  • Good Microsoft Office skills (Word and Excel).
  • Experience with sample handling in an industrial laboratory.
  • Good understanding of GLP (FDA, EMA and OECD) and GCP regulations (as applicable), as well as 21 CFR Part 11 (electronic records and electronic signatures) is desirable.
  • Excellent verbal and written communication skills.

Perform instrument maintenance, analytical method research and development, method validation and sample analysis in accordance with regulatory compliance.

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