
Quality Scientist
3 weeks ago
We have developed bespoke therapies with targeted functions to treat disease at a much lower cost than current donor-derived microbial products.
Why join us?The work we do is changing lives, and you will play a vital role in that missionWe offer a supportive, innovative environment where your contributions truly matter The opportunity to come on our journey, and develop with us globally We offer a competitive salary Role overview: The Quality Scientist is responsible for supporting product release, documentation control, deviation and CAPA management, internal audits, and periodic reviews.
The role also performs selected QC testing, including environmental monitoring, and supports validation and training activities.
Main Responsibilities Performing Quality Control (QC) testing, including microbiology, environmental monitoring, water testing, and raw material analysis Supporting product release processes through review of batch documentation and quality data Assisting in the maintenance and improvement of the Quality Management System (QMS)Managing documentation control, deviations, CAPAs, and change controls in compliance with GMPDrafting and reviewing SOPs, work instructions, and quality forms Participating in internal audits and ensuring audit readiness across departments Supporting product stability programs, quality metrics reporting, and periodic product reviews Acting as a delegate for QA or QC leads when required, ensuring business continuity Contributing to investigations and root cause analysis for quality incidents Promoting a culture of quality, compliance, and continuous improvement across teams What you will bring: Minimum 2 years' experience in a c GMP or GLP-regulated quality control laboratory A degree in microbiology, biochemistry, analytical science, or a related scientific discipline Strong understanding of quality systems, regulatory standards, and GMP compliance Experience with microbiological QC testing, environmental monitoring, or product stability testing Excellent attention to detail with strong documentation and data integrity practices Proven ability to prioritise tasks, troubleshoot issues, and contribute to continuous improvement Confident communicator with strong verbal and written skills Experience with biological therapeutics or complex biotech products is desired Familiarity with CAPA, deviations, change control and internal audits is preferred A team player mindset, willing to collaborate cross-functionally to support product quality and business continuity Join us in making a difference in microbiome therapeutics.
Click apply and upload a current Resume outlining your related experience and skills.
Please note this role is based in Adelaide, so you need to be in Australia with full working rights to be considered.
All applicants will be contacted via email in the first instance to advise if progressing or if unsuccessful.
For further information and a confidential discussion contact Michaella on 0434 983 743 / hrtalent@esshr.com.au
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