About Us

Lavida Pharmaceuticals is a TGA-licensed manufacturer of therapeutic goods based in New South Wales, Australia. We provide end-to-end manufacturing solutions for both therapeutic and non-therapeutic products. Guided by our core values—ingenuity, trust, collaboration, and accountability—we are committed to developing and delivering innovative, high-quality products that enhance health and wellbeing.

As part of our continued business growth, we are seeking an experienced Afternoon Shift(3:30pm-12am) In-Process Quality Control (IPQC) / Quality Assurance Officer to join our team. This role presents an excellent opportunity to contribute to a progressive and rewarding pharmaceutical manufacturer.

Key Responsibilities

Support the achievement of quality and broader business objectives.

Conduct in-process quality control testing and inspections at various stages of manufacturing across multiple dosage forms (including, but not limited to, solid oral dosage forms).

Perform physical testing on raw materials, intermediates, and finished products in accordance with Standard Operating Procedures (SOPs), Good Manufacturing Practice (GMP), and compendial methods.

Assist in the design, qualification, and validation of manufacturing processes and equipment to ensure suitability for pharmaceutical production.

Accurately document and record all testing activities, results, and observations in compliance with regulatory and GMP requirements.

Analyze and interpret test results, promptly reporting any deviations or non-conformances to the relevant stakeholders.

Investigate out-of-specification (OOS) and out-of-trend (OOT) results, perform root cause analysis, and support the implementation of corrective and preventive actions (CAPAs).

Provide technical support, guidance, and training to production staff on quality-related procedures.

Maintain compliance with all safety requirements and ensure a clean, organized, and GMP-compliant work environment.

Candidate Requirements

Demonstrated at least 2 years experience in quality documentation and product review within a GMP-regulated environment.

Bachelor’s degree in Science, Quality Assurance, or a related field.

Prior training in GMP and/or HACCP, with a strong understanding of compliance and safety standards.

Physically fit, reliable, and capable of meeting the physical demands of the position.

Access to reliable transport and flexibility to work on an Afternoon Shift from 3:30pm to 12am.

Legal entitlement to live and work in Australia.

Additional Information

No agencies – applications from recruitment agencies will not be accepted.

If you believe you meet the above criteria and are motivated to contribute to a dynamic and innovative pharmaceutical manufacturer, we encourage you to apply now.