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Drive Continuous Improvement as a Quality Associate
3 weeks ago
Quality Associate Position Summary
">- This role is responsible for ensuring the quality of our compounded products by driving ongoing continuous improvement in Quality performance across the site and the business.
As a key 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.
- Release compounded batches
- Participate in investigation and root cause analysis of non-conformances, supplier and customer complaints
- Contribute to risk assessment, change control, validation, internal audits, document reviews, CAPA and recall activities
- Coordinate action items related to these activities
- Develop and deliver training on Quality procedures and requirements
To be successful in this role, you will require:
- Experience in a GMP compliant pharmaceutical manufacturing environment
- Background in sterile compounding
- Desirable: Experience with regulators of pharmaceutical manufacture (e.g. TGA)
- Knowledge of continuous quality improvement
- Proficiency in common IT software (MS Word, MS Excel, MS Visio)
- Strong time and task management skills
- Tertiary qualification in a Science or relevant discipline
Additional benefits include the opportunity to thrive in a fast-paced environment where quality is paramount and develop strong leadership and role modelling capabilities.
