Quality Assurance Officer
- Perform batch, bulk product, finished product and component release, including issuing CoAs and CoCs.
- Maintain the GMP quality management system through document control, investigations, deviations, change controls and CAPAs.
- Support Product Quality Reports and vendor assurance while working with cross-functional teams and international manufacturing sites.
Quality Assurance Officer | $90K + Super | Permanent Full-Time | Pinkenba | Immediate Start Preferred | Pharmaceutical Manufacturing
We are a leading supplier of solid dose complementary medicines to many of Australia's most popular vitamin, mineral and herbal supplement brands. When we say "Healthy Begins Here," we mean that we put the health of consumers above all else — it's what drives everything we create as we find solutions for our customers and consumers.
This new opportunity is for an experienced individual who can help deliver our quality products and assist in the management of our TGA GMP standard QMS systems. You will work as part of our existing QA team, collaborating closely with our Operations, Packaging and wider teams both locally and at our China-based manufacturing plants. You will act as one of our Authorised Persons performing batch release and be part of our QMS systems management and execution.
About You & Key Responsibilities
- Perform release of bulk and finished products, and components, including issuing CoA and CoC
- Perform release of batch records to manufacture
- Draft, review and approve documents including SOPs and specifications, as well as raw materials, bulk and finished product specifications
- Maintain and control ERP codes and BOMs
- Raise, investigate and document Customer Complaints, Non-Conformances, Deviations, Change Controls and CAPAs related to products, materials and processes
- Assist in the preparation and delivery of annual Product Quality Reports, and support vendor assurance activities
- At least 3 years' experience in a regulated GMP environment, with working knowledge of PICs GMP, TGA GMP guidance documents and standards relating to AUST L and OTC medicines
- Demonstrated experience performing batch release and quality assurance investigations in a regulated GMP environment
- An understanding of PQR requirements; understanding of Vendor Assurance requirements desirable
- Strong written and verbal communication skills, with the ability to engage cross-functional teams
- High attention to detail and ability to meet tight deadlines
- A Degree or Diploma in Science or a related field desirable, along with experience using ERP systems
- A positive, "can-do" attitude and mindset to thrive in a dynamic and diverse work environment
What's on Offer?
- $90,000 + Super
- Permanent, full-time role, Monday to Friday
- Immediate start preferred
- Opportunity to advance your career within a growing pharmaceutical manufacturer
- Collaborative team environment working across local and international sites
Apply Now
If you are a dedicated professional seeking to advance your career in the pharmaceutical industry, we encourage you to apply for this opportunity. Please submit your resume and cover letter outlining your suitability for the role.
#SCR-imani-annor
#ChooseFuse
Consultant
Imani Annor
Recruitment Consultant
0468 040 731
iannor@fuserecruitment.com
https://www.sourcr.com/recruiter/imani-annor
Reference number: BH-39979
Profession:Manufacturing & OperationsQuality Assurance & Control
Company: Fuse Recruitment
Date posted: 6th Oct, 2026
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