Quality Specialist

2 weeks ago

Brisbane, Australia Icon Group Full time

**Quality and Safety**

**Brisbane**

**Full Time**

**Slade Health**

**Job Ad Summary**:
Join the Quality Assurance team operating across Australia and New Zealand | Permanent full-time role in leading manufacturer of compounded medicines | Can be based in Australia or New Zealand.

**Quality Assurance Associate / Senior Quality Assurance Associate / Quality Assurance Specialist - Slade Health**
- Be Part of An Exciting Team working in a Dynamic and Supportive Work Environment
- Play a key role in ensuring the compliant operation of a network of GMP Licensed compounding facilities, maintaining the overarching quality systems and supporting both site-based and national teams.
- Permanent Full-Time Position
- Preferably based at Geebung (QLD), but for the right applicant the role may be based at any Slade Health site with flexible work arrangements.
- Flexible Work Arrangements possible - part time working from home.

**About Slade**:
Slade Health is a leading provider of aseptically compounded chemotherapy, antibiotics, parenteral nutrition and analgesic medicines. We operate GMP Licensed manufacturing facilities in Australia (Mount Waverley VIC, Geebung QLD, Mt Kuring-gai NSW) and New Zealand (Auckland)

**About the Role**:
**Experience, Knowledge, Skills & Abilities**

You will be able to demonstrate the following:

- Experience driving Quality in a GMP licenced manufacturing environment or equivalent.
- Strong knowledge of Quality Management Systems and the compliance management of Quality Events, but not limited to:

- Document Control, Regulatory Compliance
- Non-Conformance, Deviations, Complaints and Recalls
- Risk Management, CAPA & Change Control
- Validation, Training, Supplier Interaction and Management, Audit
- Customer Interaction and Management
- Quality Assurance Team Finance & Reporting
- Continuous Improvement, Workplace Health & Safety
- Project Management, Area Leadership
- People Management and Development
- Experience in Good Manufacturing Practice, PIC/S and the Regulatory frameworks for Scheduled drugs and wholesaling of medicines
- Strong analytical skills and experience managing data sets.
- Advanced skills in MS Excel, intermediate skills in the general MS Office suite
- Ability to communicate effectively with peers, management and externally with customers, suppliers and when required regulatory bodies.
- Strong task and time management skills. You will work in a fast-paced environment, and you will need to be able to effectively co-ordinate, track and prioritise tasks to deliver to tight timeframes.

This role is offered on a permanent full-time basis working 76 hours per fortnight.

**How to Apply**:

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