Do you have skills in managing and maintaining documents and records? Do you have a keen eye for detail? Are you looking to take your career to the next stage supporting research of new medicines?
If so, you’ll fit right in at Crux Biolabs.
Our company is growing fast – and we’re expanding our Quality Control team.
What does that look like? You’ll be a critical player, checking clinical trials records to ensure the highest data integrity for pharma companies creating medicines that save lives.
Driven by science, respected for results
At Crux Biolabs, we love one thing: science. It’s what unites us and drives us to help our clients create safe and effective medicines the world can access. Since day one in 2011, we’ve supported clinical and pre-clinical pharmaceutical development projects from Australia and around the globe. Our team is small – 34 to be exact – but our results speak volume. That’s why we work with some of the best pharmaceutical and biotech companies and clinical research organisations.
The Crux Biolabs evolution
Like the human cells we analyse, Crux Biolabs is growing fast. We’re on the hunt for team members to be a part of our growth. People are excited to join Australia’s pharmaceutical and clinical development ecosystem – at the ground level.
What does that mean for you? Ample opportunity to innovate. And a career trajectory that matches our expanding horizons.
The culture that awaits you inside Crux Biolabs
Fast-paced: Your attention to detail will keep us running at peak performance.
Innovative: We love staff who look for ways to improve efficiency.
Supportive: Thrive in a culture that values inclusivity and development. Your ideas are heard, your efforts applauded, and your successes celebrated.
Rewarding: Work hard and be rewarded with a competitive salary and flexible work arrangements.
Impactful: This isn't just another job – it's an opportunity to shape how we work and leave a lasting impression on a growing Australian industry.
A day in your new work life
As a Quality Control Associate, you’ll be responsible for managing and maintaining clinical trials data. That means you’ll be:
- Quality controlling data and reports
- Resolving data discrepancies
- Transferring data to clinical clients
- Archiving records
And best of all? You can park onsite.
What we’re looking for
To be a top pick, you’ll need to love being organised, be a master of the minutiae, and enjoy working in a team.
At least two years of experience in a similar role is ideal.
Ready to join the Crux Biolabs team?
If you’re looking to grow your career, this is the moment you’ve been waiting for.
This role will require you onsite, Monday – Friday (day shift). We can be flexible for the right candidate. To be considered, you must be an Australian citizen, permanent resident or have an appropriate working visa.
We welcome and encourage applications from individuals of Aboriginal and Torres Strait Islander descent, as well as from all members of the LGBTQI community.
Ready to apply? Then please send us a cover letter (telling us how your experience relates to this role) and a brief resume.
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