Quality Manager – Pharmaceuticals & Clinical Trial Supply
i-Pharm Consulting · Melbourne
Job description
About the role
Join a specialist pharmaceutical sourcing and clinical‑trial supply business operating across Australia, Singapore, Japan and New Zealand. Reporting to the Director of Supply Chain & Quality, you will own day‑to‑day Quality operations and lead a small team.
Key responsibilities
- Manage and develop two Quality team members, setting priorities and providing guidance.
- Own and maintain the Quality Management System, including procedures, deviations, CAPA and continuous improvement.
- Plan and coordinate internal audits and support external audits.
- Oversee supplier qualification, audits and quality agreements.
- Provide Quality oversight across pharmaceutical sourcing, storage and distribution through external partners.
- Support assessment and resolution of temperature excursions, traceability issues and other product quality concerns.
Required profile
- Strong experience in pharmaceutical Quality Assurance, preferably within clinical‑trial supply or distribution.
- People‑management experience with the ability to guide a small team.
- Confidence to take ownership, exercise sound judgement and work independently.
- Commercially aware approach balancing compliance and operational needs.
Required skills
- Management of QMS, CAPA, deviations and audits.
- Supplier qualification and quality agreement handling.
- Understanding of Good Distribution Practice (GDP) and Good Wholesaling Practice (GWP).
- Familiarity with outsourced GMP packaging and labelling activities.
What we offer
- Salary $130,000–$150,000 plus super.
- Melbourne CBD location.
- Ownership of the day‑to‑day Quality function.
- Leadership of a team of two Quality professionals.
- Exposure to international operations and the chance to shape developing Quality systems.
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Published 1 hour ago
Expires 1 month from now
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i-Pharm Consulting
Melbourne
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