QA Professional

5 days ago

Melbourne, Victoria, Australia beBeeQuality Full time $90,000 - $140,000

About Us
At IDT Australia, we provide globally recognised pharmaceutical development and GMP manufacturing services. With a strong focus on cancer and mental health therapies, we support the development of novel medicines for clinical trials through R&D, process scale-up, and sterile manufacturing. Our facilities are TGA and FDA accredited.

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  • We are seeking a highly skilled and strategically minded QA professional to join our Quality team. This role is designed for professionals who bring deep expertise in organisational analysis, quality systems, and change facilitation within a GMP-critical environment.
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Skills & Experience Required

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  1. Advanced expertise in organisational systems and quality frameworks within a GMP-regulated pharmaceutical environment is required. The ideal applicant will demonstrate:">
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  • Proven experience in change management facilitation, particularly in implementing quality systems and continuous improvement initiatives.">
  • Strong capabilities in quality auditing, including vendor assurance, documentation review, and regulatory compliance.">
  • Experience in skills auditing and workforce capability analysis to support operational excellence.">
  • Proficiency in industry analysis, with the ability to evaluate and optimise manufacturing and quality processes.">
  • Exceptional analytical and problem-solving skills, with a track record of contributing to successful organisational improvement initiatives.">
  • Advanced communication and stakeholder engagement skills, with the ability to influence cross-functional teams and drive strategic outcomes.">
  • Project management experience in complex pharmaceutical environments, including sterile manufacturing and novel therapy development.">
">Tertiary qualifications in Pharmacy, Science, Engineering, or a related discipline.">Minimum 5 years' experience in a quality, compliance, or organisational improvement role within the pharmaceutical or life sciences sector.">Demonstrated ability to work autonomously and lead quality initiatives across multiple projects.">

Additional Requirements

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  1. The ideal candidate should have advanced knowledge in organisational systems and quality frameworks within a GMP-regulated pharmaceutical environment.">
  2. They should be able to facilitate change and implement quality systems and continuous improvement initiatives.">
  3. The candidate should also have experience in quality auditing, skills auditing, and workforce capability analysis.">
  4. Advanced communication and stakeholder engagement skills are essential for influencing cross-functional teams and driving strategic outcomes.">
  5. Project management experience in complex pharmaceutical environments is also desirable.">

Why Choose This Role?

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  • This QA Associate role offers the opportunity to work in a dynamic and challenging environment, supporting the development of novel medicines for clinical trials.">
  • The ideal candidate will have the chance to contribute to successful organisational improvement initiatives and drive strategic outcomes.">
  • They will also have the opportunity to work autonomously and lead quality initiatives across multiple projects.">
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