Tasks & Responsibilities
- Managing all quality aspects including technical Quality Agreements and product listing update.
- Third party management including supplier qualification and risk assessments, Supplier Quality Audits, Vendor Qualification, Vendor Management.
- Internal and external audit activities and follow up on corrective actions ensuring continuous improvement of systems and procedures.
- Complaint handling.
- Batch release management.
- Stability program management.
- Writing and drafting processes, preparation and review/approval of area documentation (SOPs, methods), Training.
- QMS Maintenance, implemented QMS on site.
- Audit of production and QC documentation
- Assist the assessment and management of documents of the quality system e.g. deviations, change controls and CAPAs
- Assist in internal audits and in the review of validation reports
Selection Criteria
- Tertiary qualified in complementary science or related discipline
- Previous experience in the Pharmaceutical industry in a QA role
- Previous experience in the assessment of deviations, change controls and CAPAs
- Demonstrated knowledge of quality systems
- Excellent written and verbal communication skills
- High attention to detail
- High motivation, flexible and adaptable
- Computer literacy including Word and Excel knowledge
- Eligible working visa in Australia
Job Types: Full-time, Permanent
Pay: $55,000.00 – $70,000.00 per year
Language:
- Mandarin (Preferred)
Work Authorisation:
- Australia (Preferred)
Work Location: In person
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