Progressive and Far-Reaching Career OpportunitiesCollaborative and Supportive Work Environment9 AM - 5 PM Monday to Friday - Permanent Full-Time Position – Mt Kuring-gai LocationQUALITY ASSOCIATE – SLADE HEALTH, MT. KURING-GAISlade HealthUnderpinned by 60 years' experience, Slade Health is Australia's leading chemotherapy compounding provider with a commitment to patient care, quality, innovation and integrity.Slade delivers approximately 1.2 million infusions each year to over 200 hospitals across the public and private healthcare sector, including long-term state-wide government contracts.
Slade operates five licensed manufacturing facilities - four in Australia and one in Current Zealand, and under Icon Group has recently acquired BathASU (part of Pharmaxo Group) in the United Kingdom.
(AM1)Slade Health is a full-service compounder providing antibiotics, chemotherapy, analgesics and theatre lines, and the exclusive compounder in Australia of Fresenius Kabi Total Parenteral Nutrition.For more information visit ;The OpportunityAs an integral member of the Quality team, you will report to the Site Quality Manager and work closely with Operations to ensure that the compounding centre operates in compliance with regulatory and GMP requirements ensuring that the products compounded are of the highest quality.
This is a permanent full-time position working 76 hours a fortnight, Monday to Friday between the hours of 9 AM and 5 PM.Key ResponsibilitiesEnsure all incidents, deviations and complaints are reported to the appropriate persons and registered in the QMS in a timely fashion.Investigation and root cause analysis of non-conformances, supplier and customer complaintsWriting of customer complaint responses and monthly reportsParticipating in risk assessment, change control, validation, internal audits, document reviews,



CAPA and recall activitiesConduct training for staff against Quality procedures and requirements.Ensure training records are complete for all training against Quality procedures.Provide advice and guidance to staff regarding quality processes and procedures when requested.About YouExperience in a GMP compliant pharmaceutical manufacturing environmentExperience in a sterile compounding environmentExperience in development and application of Quality SystemsExperience with regulators of pharmaceutical manufacture (eg TGA)Experience in continuous quality improvementCompetencyin common IT software (MS Word, MS Excel, MS Visio)Competent in project, time and task managementTertiary qualification in a Science discipline (preferably including study in microbiology or chemistryThe successful candidate will thrive in a fast-paced environment where quality is paramount.
You will have a proactive approach, exceptional communication skills and be a strong leader/role model.In addition, you will support the team with Environmental Monitoring activities and perform quality assessments quarantined incoming goods as required.
You will drive ongoing continuous improvement in Quality performance across the site and the business.
This means identifying key areas of focus and implementing improvements to raise compliance and efficiency and engaging with stakeholders to promote the Quality culture.Excited to join us?
Our team makes us who we are, they shape our impact and drive our success.
Visit en/careers/our-people/stories/ to read the stories of our incredible people.
Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees.
We encourage applications from all diverse backgrounds.Icon is committed to managing the risk of transmission of specified vaccine preventable diseases (VPDs) including COVID-19.
Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.
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📌 Quality Associate (Sydney)
🏢 Icon Group
📍 Sydney