Quality Associate
2 weeks ago
**Pharmacy Compounding**
**Auckland - New Zealand**
**Full Time**
**Slade Health**
- **Dynamic, Collaborative** and **Supportive** Work Environment
- Progressive and Far-Reaching Career Opportunities - Exciting Expansion into New Zealand **(Brand New State of the Art Facility)**:
- **Full Training is Provided** on the Job and Development Support is Ongoing
- **Permanent Full-Time Position** - Auckland, NZ Location
- Monday to Friday - between 8am
- 6pm - **Free On-Site Parking**
**About Slade Health**:
Slade Health, a division of ICON Group, is one of Australia’s largest providers of sterile compounding services, including chemotherapy, analgesics, antibiotics and TPN products.
Slade Health supplies over one million infusions per annum to in-excess of 200 hospital partners via its three compounding facilities. It is now poised for its next phase of growth, creating exciting new opportunities within the organisation in New Zealand.
**Slade Health New Zealand**:
Slade Health is partnering with the Auckland District Health Board (ADHB) to build a new world-class Medsafe licenced compounding facility capable of producing chemotherapy, antibiotics, analgesics, and nutritional products.
The partnership with ADHB will see Slade Health supply compounded products for public hospitals in the Auckland region, which represents approximately 40% of New Zealand’s cancer patients.
**About the role**:
As an integral member of the Quality team, the Quality Associate Releaser will report to the Site Quality Manager and work closely with Operations to ensure that Avondale’s 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 80 hours a fortnight.
**Key Responsibilities**:
- Releasing 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.
**What we are looking for**:
- Work history in a GMP compliant, sterile pharmaceutical manufacturing environment
- Experience with regulators of pharmaceutical manufacture (eg TGA)
- Competency in common IT software (MS Word, MS Excel, MS Visio)
- Competent in time and task management
- Preferable - tertiary qualification in a Science discipline
**How to apply**:
COVID Health Requirement
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