Australian Pharmavet Contract Manufacturing Pty Ltd (Pharmavet) has an inherent competitive advantage in Production Planning, Operations and Quality Assurance deliverables in line with industry standards. Pharmavet is a fully accredited APVMA licenced manufacturing facility and holder of a schedule 4 drug manufacturing licence.

We are a small group of collective like-minded individuals who love to chase big goals and have fun along the way. With an unrelenting focus on growth, continuous improvement, and commitment to our team members, Pharmavet provides real opportunities for passionate, high achieving people who bring their authentic self to work. We are continuing to build our high-performing team, that has collaboration, transparency, and an innovative mindset, at the heart of everything they do.

Pharmavet is a rapidly growing contract manufacturer of Animal Health products, and its employees are the core of its growth. We’re a progressive, and autonomous organization.

We are an expanding APVMA-accredited, GMP veterinary pharmaceutical manufacturer, and need an enthusiastic Quality Control Officer to join our team.

This is a part-time contact role for 3 months with the possibility of extension. Working two days a week Monday and Tuesday 7.30am to 3.30pm.

Responsibilities:

Physically check raw materials and packaging materials for compliance with quality standards.

Perform quality pass checks for BOM kits, ensuring all materials meet required specifications.

Verify transfer documents and certificates of analysis (COA) against packaging specifications.

Accurately book in Bill of Materials (BOM) kits in Q Master and MYOB systems.

Ensure all entries are completed in a timely and precise manner.

Conduct in-process checks at multiple stages of production to ensure adherence to quality standards.

Perform in-process testing on both in-process and finished products, documenting results accurately.

Perform sampling processes and coordinate sample testing with external laboratories.

Assist in the reconciliation process with production teams to ensure all materials are accounted for correctly.

Accurately record and manage inventory transactions related to quality control activities.

Manage the process of handling returns back of Finished products, ensuring proper documentation and compliance with quality standards.

Strict adherence to APVMA & GMP Code of ethics for the pharmaceutical industry. Provide support during inspections and audits.

Serve as a subject matter expert for QC-related tasks, providing guidance and support to the production and quality teams.

Handle multiple tasks in a timeline-driven environment, ensuring all quality control activities are completed accurately and on time.

Qualifications:

1-2 years of prior work experience in a QA/QC area under GMP, APVMA, TGA regulated industry preferred, but training will be provided.

A Bachelor's degree, diploma in scientific area is preferred but an exception may be made for the right candidate.

Must be able to work as part of a team.

Fast learning nature, positive attitude and good communication skills.

Has attention to detail with good organizational skills.

Must be proficient with Microsoft Office applications.