Quality Associate
vor 1 Monat
Pharmaceutical Compounding Sydney Full Time - Slade HealthQUALITY ASSOCIATE - RELEASERSlade Health, Mount Kuring Gai, Sydney - NSWDynamic, Collaborative and Supportive Work EnvironmentProgressive and Far-Reaching Career Opportunities - State of the Art FacilityTwo Permanent Full-Time Positions availableShifts:First: 8:00 AM to 4:00 PMSecond: 2:00 PM to 10:00 PMBoth roles subject to roster changes, Monday - Friday and some weekends.
Location: Mount Kuring Gai (Sydney), NSW.About Us:Slade Health is a provider of sterile compounding services from its TGA licensed manufacturing facilities based in Queensland, New South Wales, Victoria, and New Zealand.
As a well-established and respected industry name, Slade has been producing aseptically compounded pharmaceutical products for over 50 years.Part of something bigger:Being part of Icon Group, Australia's largest dedicated cancer care provider, with a global presence in Singapore, Mainland China, Hong Kong, and New Zealand.The Opportunity:As an integral member of the Quality team, you will report to the Quality Pharmacist Supervisor and work closely with Operations to ensure compliance with regulatory and GMP requirements.
This is a permanent full-time position working a minimum of 76 hours a fortnight, Monday to Friday and some weekends, with shifts to support operations.Key Responsibilities:Releasing of compounded batches.Participate in investigation and root cause analysis of non-conformances, supplier and customer complaints.Participate in risk assessment, change control, validation, internal audits, document reviews, CAPA, and recall activities.Liaise with relevant stakeholders to complete action items related to the above.Conduct and coordinate training on Quality procedures and requirements.Additionally, you may support the team with Environmental Monitoring activities and perform quality assessments of quarantined incoming goods as required.
You will drive ongoing continuous improvement in Quality performance across the site and the business.About You:Experience in a GMP compliant pharmaceutical manufacturing environment.Experience in a sterile compounding environment.Experience with regulators of pharmaceutical manufacture (e.g., TGA) desired.Experience in continuous quality improvement.Competency in common IT software (MS Word, MS Excel, MS Visio).Competent in time and task management.Tertiary qualification in a Science or relevant discipline.Good communication skills.We invite you to apply if you are excited to join our team and make a differenceIcon 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).
Certain roles may require the successful candidate to show evidence that they have been vaccinated against or are not susceptible to specified VPDs.#J-18808-Ljbffr
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