In-Demand Quality control Jobs in Logan City Qld

Quality Auditor
Breathe Life Sciences —Meadowbrook QLD
- $80,000 - $90,000 a year
- Full-time
- Bachelor's degree
- Organisational skills
- In-person
Quick Apply
7d
Laboratory Technician
MAAS Group —Luscombe QLD
- Nights as needed
- Laboratory
- On-the-job training
Quick Apply
3d
Production Supervisor
KG Talent —Richlands QLD
- Full-time
- Leadership
- Communication skills
Quick Apply

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Quality Assurance Manager
Knotwood PTY LTD —Stapylton QLD
Investigate quality issues, non-conformances, and customer concerns. Assist with supplier quality management and incoming material standards.
$80,000 a year
Quick Apply
4d
Quality Auditor
Breathe Life Sciences —Meadowbrook QLD
Minimum of 2 years of experience in quality assurance, quality control, or audit roles within the pharmaceutical, biotechnology, or related regulated industry.
$80,000 - $90,000 a year
Quick Apply
7d

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Quality Auditor

Breathe Life Sciences
Meadowbrook QLD

Quick Apply

Job Details

Full-time
$80,000 - $90,000 a year
7 days ago

Qualifications

Quality assurance
Bachelor's degree
Organisational skills
Pharmacy

Full Job Description

Breathe Life Sciences (BLS) is a TGA-licensed pharmaceutical manufacturer based in Meadowbrook, Queensland. We operate under Good Manufacturing Practice (GMP) frameworks including PIC/S PE 009.

A full-time position is currently available within the company for an experienced Quality Auditor to join our Quality and Regulatory team. Working closely with cross-functional teams, you will play a crucial role in maintaining the highest standards of quality assurance and compliance across our manufacturing operations.

Key duties of the role:

Lead internal audits and ensure continual audit readiness in production and warehouse, inspections, and quality management system reviews to ensure ongoing compliance with TGA regulations, GMP guidelines (PIC/S PE 009), and other relevant standards.
Analyse organisational methods, processes, and workflows across manufacturing and quality functions to identify inefficiencies, non-conformances, and opportunities for improvement.
Review and audit standard operating procedures (SOPs), batch records, validation protocols, and other GMP documentation for compliance, accuracy, and completeness.
Perform deviation investigation, root cause analysis, and trending to identify and resolve quality issues, and implement corrective and preventive actions (CAPAs).
Conduct risk assessments and recommend systemic improvements to enhance product quality, operational efficiency, and regulatory compliance.
Prepare audit reports, trending analyses, and management review inputs for senior leadership.
Provide training and guidance to team members on quality systems, regulatory requirements, and best practices in quality assurance.
Collaborate with manufacturing, research and development, and regulatory affairs teams to support product development, scale-up, and commercialisation activities.
Maintain and update audit records, documentation, and reports in accordance with regulatory requirements and company policies.
Uphold a culture of quality and compliance through effective communication, training, and adherence to established standards.

Skills and experience required:

Bachelor’s degree in Chemistry, Pharmacy, Biotechnology, or related field; advanced degree preferred.
Minimum of 2 years of experience in quality assurance, quality control, or audit roles within the pharmaceutical, biotechnology, or related regulated industry.
Strong knowledge of TGA regulations, GMP guidelines, and international quality standards (e.g. ICH, USP, EP).
Demonstrated experience in conducting internal and external audits, inspections, and regulatory submissions.
Excellent attention to detail, organisational skills, and the ability to prioritise and manage multiple tasks effectively.

Job Type: Full-time

Pay: $80,000.00 – $90,000.00 per year

Work Location: In person

Quick Apply

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