Scientist I, Flow Cytometry (Brisbane)

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

 

·     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.

• Master’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 and FlowJo is desirable.

• Detail-oriented and responsible.

• Ability to work effectively in a team as well as independently.

• Strong collaboration, time management, and organisational skills.

• Good Microsoft Office skills (Word and Excel).

• Experience with sample handling in an industrial laboratory.

• Good understanding of GLP regulations (FDA, EMA, and OECD), GCP regulations (as applicable), and 21 CFR Part 11 requirements for electronic records and electronic signatures is desirable.

• Excellent verbal and written communication skills.