Onsite QA Associate - GMP Pharma, Impact & Growth

PharmaCare Group

Sydney

On-site

AUD 75,000 - 100,000

Full time

38 hours ago
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Benefits offered by this job

Salary continuance
Private health insurance
Parental leave
Training & development
Onsite parking

Job summary

PharmaCare is seeking a QA Associate to ensure safety and quality of medicines, overseeing pre- and post-production activities. The role emphasizes GDP, batch release, documentation control and CAPA investigations in a GMP environment.

The ideal candidate will have 3–5 years’ QA/QC experience, strong English communication, and the ability to work across functions, with a keen eye for detail and a proactive, reliable attitude.

Qualifications

  • Tertiary qualifications in a Science related discipline.
  • Experience in a GMP/QA environment within pharmaceutical manufacturing.
  • Experience with batch release and documentation control.
  • Experience with internal auditing and CAPA processes.
  • Knowledge of GMP guidance and Australian Code.

Responsibilities

  • Review batch documentation to support batch release and RFS.
  • Issue batch documentation to production and maintain traceability.
  • Perform environmental monitoring sampling and testing activities.
  • Maintain master documentation control and change records.
  • Participate in internal audits and CAPA investigations.
  • Update procedures and SOPs, and support training programs.
  • Manage retention and testing of raw materials and finished goods samples.

Skills

GMP knowledge
Batch release
Documentation control
Internal auditing
CAPA investigations
Sampling and inspection
Environmental monitoring
ILAB system
MRP/ERP systems
Microsoft Office

Education

Science degree or related qualification

Tools

ILAB system
MRP/ERP systems
Microsoft Office

Job description

PharmaCare is seeking a QA Associate to ensure safety and quality of medicines, overseeing pre- and post-production activities. The role emphasizes GDP, batch release, documentation control and CAPA investigations in a GMP environment.

The ideal candidate will have 3–5 years’ QA/QC experience, strong English communication, and the ability to work across functions, with a keen eye for detail and a proactive, reliable attitude.

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