Homart Group is a leading Australian company specialising in the development, manufacturing and global marketing of high-quality, Australian-made health supplements, skincare, functional dairy, and pet supplements.
Building on a proud 30-year history, Homart has entered an exciting new chapter. In late 2024, we enhanced our portfolio by acquiring renowned heritage brands Thompson's Herbals and Thursday Plantation. To fast-track our direct-to-consumer (B2C) footprint, we also welcomed the premium wellness brand Salt Lab to the family at the end of 2025.
About the role
We are seeking an enthusiastic, positive, and growth-oriented QA/QC Officer who is eager to learn, contribute, and excel. Working as an integral part of our QA/QC Team, you will assist with all tasks and functions across GMP, HACCP, Regulatory Affairs, New Product Development, Formulating, Technical, and QA/QC systems.
This is a unique opportunity that demands dedication, persistence, and innovation. For the right candidate, this role is a stepping stone, offering the distinct capability to transition into Senior Roles as the company grows.
Key Responsibilities:
- Quality Management: Manage all quality aspects, including updating technical Quality Agreements.
- Vendor & Supplier Management: Oversee third-party qualification, risk assessments, supplier quality audits, and ongoing vendor management.
- Audits & Compliance: Lead internal and external audit activities, follow up on corrective actions, and drive the continuous improvement of systems and procedures.
- QMS Oversight: Implement and maintain the site Quality Management System (QMS), and audit production and QC documentation.
- Documentation & Training: Write, draft, review, and approve area documentation (SOPs, methods) and facilitate team training.
- Daily QA Operations: Manage batch releases, oversee the stability program, and handle customer complaints.
- System Assistance: Support the assessment and management of quality system documents, including deviations, change controls, CAPAs, and the review of validation reports.
Requirements & Qualifications:
- Tertiary qualification in a complementary science or a related discipline.
- Proven experience within a QA role inside the Pharmaceutical industry in highly regarded.
- Demonstrated knowledge of quality systems, with hands-on experience assessing deviations, change controls, and CAPAs.
- High attention to detail, strong motivation, flexibility, and adaptability.
- Excellent written and verbal communication skills.
- High computer literacy, including proficiency in Microsoft Office Suite.
How to Apply
If you are a detail-oriented, self-driven QA/QC professional who is passionate about compliance and excellence, we would love to hear from you!
Please submit your resume and a cover letter outlining your relevant experience and achievements.
Benefits:
Ability to commute/relocate:
- Rydalmere NSW: Reliably commute or planning to relocate before starting work (Required)
Application Question(s):
- What's your expected annual base salary?
- How much notice are you required to give your current employer?
- Could you please provide a few dates and times you are available for a one-hour, in-person interview?
Work Authorisation:
Work Location: In person
