Pharmaceutical Compounding
Brisbane
Full Time
Slade Health
Supportive and Collaborative Team Environment Permanent full-time position – 9:54am to 6pm, Monday to Friday (Shift times may vary depending on roster) Be Part of An Exciting Team working in a Dynamic and Supportive Work Environment Play a key role in ensuring quality compliant operations are maintained at all sites About Slade:
Slade Health is a national sterile compounding service provider with TGA accredited manufacturing facilities based in Victoria, Queensland, New South Wales, South Australia and New Zealand. As a well-established industry name, Slade has been producing aseptically compounded pharmaceutical products such as chemotherapy drugs for use by patients in hospitals for over 50 years.
About the role:
As an integral member of the Quality team, you will report to the Quality Pharmacist Supervisor and site Quality Manager 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. You will contribute to ongoing continuous improvement in Quality performance across the site. This means implementing improvements to raise compliance and efficiency and engaging with the production team to promote the Quality culture.
This is a permanent full-time position working a minimum of 76 hours a fortnight 9:54am to 6pm, Monday to Friday (Shift times may vary depending on roster).
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.
In addition, 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. This means identifying key areas of focus and implementing improvements to raise compliance and efficiency and engaging with stakeholders to promote the Quality culture.
What we are looking for: 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 discipline.
You 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.
The successful candidate will have a can-do and patient-centric attitude, strong work ethic and great communication and influencing skills to build fruitful relationships within the business. It is important that you are a collaborative person and flexible, able to face last minute changes of schedule.
How to apply:
If you think you have the skills we are looking for, then we want to hear from you! Please apply by clicking on the link below – a covering letter and resume must be attached.
Icon Group celebrates diversity and is committed to creating an inclusive workplace for all employees. We encourage applications from all diverse backgrounds.
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