Scientist I Immunoassay- Brisbane

Resolian Bioanalytics; Brisbane; Sur place; AUD 70 000 - 110 000; Plein temps

Résumé du poste

Resolian Bioanalytics in Brisbane seeks an experienced laboratory scientist to support GLP/GCP compliant data generation and method development. You will ensure regulatory adherence, document methods, and review data with study teams.

The role requires strong communication, attention to detail, and the ability to work both independently and within cross-functional teams in a fast-paced laboratory environment.

Qualifications

• Associate degree or higher with at least 5 years of relevant work experience.
• Ability to work in a fast-paced and dynamic environment.
• Excellent verbal and written communication skills.
• 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).

Responsabilités

• Comply with laboratory health and safety standards.
• Process, evaluate, review and interpret data results
• Research, design and develop analytical methods, includes troubleshooting of assays.
• Analyse samples following validated analytical methods.
• Maintain accurate and detailed experimental records, review data, and contribute to technical reports.
• Operate analytical instruments and associated software systems.
• Carry out routine calibration and maintenance of instruments.
• Drafting/reviewing SOPs, methods and reports.
• Collaborate across teams, departments, and sites.
• Participate in ongoing laboratory and regulatory training.
• Train and mentor junior level scientists.
• Collaborate closely with project teams, study directors/PI, and QA to ensure timely and high-quality study delivery.
• Assists with any additional tasks as assigned by management
• Partake in laboratory housekeeping duties, prepare buffers and reagents.
• Perform quality control checks

Connaissances

GLP/GCP

Data handling

Communication skills

Detail oriented

Team collaboration

Time management

MS Office

Formation

Associate degree or higher

Outils

Microsoft Word

Microsoft Excel

Description du poste

• 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.
• Process, evaluate, review and interpret data results
• Research, design and develop analytical methods, includes troubleshooting of assays.
• Analyse samples following validated analytical methods.
• Maintain accurate and detailed experimental records, review data, and contribute to technical reports.
• Operate analytical instruments and associated software systems.
• Carry out routine calibration and maintenance of instruments.
• Partake in laboratory housekeeping duties, prepare buffers and reagents.
• 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 as assigned by management

Requirements

Skills, Education & Qualifications

• Associate degree or higher with at least 5 years of relevant work experience, or an equivalent combination of education, training, and experience as deemed appropriate by management.
• Ability to work in a fast-paced and dynamic environment.
• Excellent verbal and written communication skills.
• 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).