Are you experienced in reviewing quality or batch documentation in a regulated environment?
This expanding life science organisation is seeking a committed Quality Assurance Associate to support their Quality Assurance function and ensure documentation excellence across the business.
This role is also suitable for people with a strong Quality or data review background in food and drink or the medical device and similarly regulated industries.
Reporting to the Quality Assurance Manager, you will play a critical role in maintaining compliant, accurate, and well controlled documents, data, and records.
Key Responsibilities
Review quality and batch documentation with accuracy and attention to detail
Provide document control functions, support, and guidance across the business
Maintain trackers and generate accurate status reports to support batch compilation activities
Support document archiving, ensuring controlled and compliant material movement
Coordinate SOP review cycles and ensure revisions meet required timelines
Ensure all documents are updated,



mastered, and maintained according to established procedures
Contribute to GMP compliance activities and continuous QA improvement
Requirements
Experience in document review within a regulated GMP environment is preferred but they will consider people from an ISO **** or ISO***** background.
Solid written and verbal communication skills at all levels
Knowledge of Quality Systems (desirable)
Excellent organisational skills, with the ability to work independently and as part of a team
Analytical approach to problem solving and decision making
Proficiency in Microsoft Office and confident data entry skills
We believe in the power of science - that's why we stay at the forefront of the life sciences industry, keeping up to date with the latest research, innovations, and market trends to provide valuable insight and guidance to our clients and candidates.
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📌 Qa Associate (Perth)
🏢 Impellam Group
📍 Perth