Quality Associate
vor 2 Wochen
Dynamic, Collaborative and Supportive Work EnvironmentProgressive and Far-Reaching Career Opportunities - State of the Art FacilityPermanent Full-Time Position (8AM to 4PM)– subject to roster changes, Monday - Friday and some weekends – Mount Kuring Gai (Sydney), NSW LocationQUALITY ASSOCIATE - RELEASER – SLADE HEALTH, MOUNT KURING GAI SYDNEY - NSWAbout Us:Slade Health is a provider of sterile compounding services from its TGA licenced 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 including chemotherapy, analgesic, nutrition and antibiotic drugs for use by patients in hospitals for over 50 years.Our focus on quality, service and productivity has enabled opportunities for Slade to expand significantly.
This is evidenced by our first international facility opening in New Zealand in September 2022, with our new site in Woodville SA.
With growth comes career opportunitiesThe OpportunityAs an integral member of the Quality team, you will report to the Quality Pharmacist Supervisor and work closely with Operations to ensure that the compounding centre operates in compliance with regulatory and GMP requirements and that the products compounded are released to the highest quality.
This is a fantastic opportunity to expand your current skill set and support the Quality processes we have in place.
This is a permanent full-time position working a minimum of 76 hours a fortnight, Monday to Friday and some weekends, work on shifts to support operations.Key ResponsibilitiesReleasing of compounded batches.Participate in investigation and root cause analysis of non-conformances, supplier and customer complaints.Participating in risk assessment, change control, validation, internal audits, document reviews, CAPA and recall activities.Liaising with relevant stakeholders to complete action items related to the above.Conducting and coordinating training on Quality procedures and requirements.In addition, you may 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.About YouExperience in a GMP compliant pharmaceutical manufacturing environmentExperienced in a sterile compounding environmentExperience with regulators of pharmaceutical manufacture (eg TGA) desiredExperience in continuous quality improvementCompetency in common IT software (MS Word, MS Excel, MS Visio)Competent in time and task managementTertiary qualification in a Science or relevant disciplineGood communication skillsYou will know that a successful person in this role is someone who can thrive in a fast-paced environment where quality is paramount, whilst displaying a proactive approach, exceptional communication skills, strong leadership and role modelling capabilities.Excited to join us?Our team makes us who we are, they shape our impact and drive our success.
So Apply Now and make it happen with Icon.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.#J-18808-Ljbffr
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