Research Associate

About the Company

Triton Biosensors is an international specialist in electrochemical cell technology and biosensor development. Its product portfolio includes the Sentia wine testing system, with both the analyzer and test strips, as well as the Xprecia Prime coagulation testing system, including analyzers and PT/INR test strips. The company operates a modern GMP facility in Rowville, Melbourne, and supplies products globally under ISO 13485 and other regulatory requirements such as TGA, FDA, and EU IVDR.

About the Role

This is a full-time Research Associate position supporting quality control laboratory operations and scientific investigation work in a regulated environment. The role reports to the R&D Manager and suits someone who enjoys research, innovation, quality, and compliance-driven work.

Key Responsibilities

• Carry out routine and non-routine testing and analysis of raw materials, in-process material, finished goods, and stability samples according to approved methods and specifications, working with limited supervision.
• Mix and prepare solutions needed for production and laboratory testing activities.
• Install, run, calibrate, and service laboratory instruments in line with cGMP expectations, including safety inspections and arranging repairs when necessary.
• Contribute to the creation and ongoing improvement of procedures for production support, calibration, quality control testing, and batch release work.
• Assist with batch release testing by checking results against acceptance limits and completing quality documentation accurately.
• Examine out-of-specification and out-of-trend outcomes, help identify root causes, and support CAPA actions when needed.
• Assess QC records such as test methods, worksheets, validation files, and batch release paperwork.
• Support internal and external audit activities and help close audit findings within required timelines.
• Manage laboratory equipment, consumables, and stock levels while maintaining compliance with GMP, ISO 13485, and ISO 9001 standards.
• Handle the safe storage, use, and disposal of chemicals and biological materials.
• Work with internal stakeholders and provide technical input where required.
• Keep laboratory spaces clean, orderly, safe, and compliant, and ensure waste is removed promptly and correctly.

Requirements

• A degree in a science-related field.
• Between 1 and 3 years of experience in a laboratory or research environment.
• Solid understanding of scientific concepts and statistical analysis.
• Ability to work safely with biohazardous materials.
• Exposure to QMS expectations and regulatory standards.
• Strong capability in problem-solving, organisation, and written reporting.
• Previous work in a cGMP or GLP setting will be viewed favourably.

Why Join Us

You will be part of a team of motivated professionals in a collaborative workplace that prioritises innovation, safety, and ongoing improvement.

Application Note

The role is full-time and based onsite in Rowville, Victoria, Australia. Interested candidates are invited to apply via the provided application channel.