I-Pharm is proud to be working with a highly regarded organisation at the forefront of radiopharmaceuticals, specialising in nuclear medicine and diagnostic imaging. With a strong presence across Australia and the Asia-Pacific region, this company plays a critical role in delivering life-saving diagnostic and therapeutic solutions.

They are currently seeking a dedicated Quality Assurance professional to join their team as a QA Associate. This role is ideal for someone with a keen eye for detail, a passion for maintaining the highest quality standards, and a desire to contribute to a highly regulated and technical environment.

In this position, you will be responsible for ensuring compliance with GMP and regulatory requirements, supporting quality systems, and collaborating with cross-functional teams to uphold safety and quality in radiopharmaceutical manufacturing.

If you’re looking to grow your career in a company that values technical excellence and plays a vital role in patient care, this full-time permanent role offers a fantastic opportunity to make a meaningful impact.

Responsibilities:

• Issuing system report numbers.
• Conducting system effectiveness reviews.
• Leading or participating in quality meetings, including change control and deviation management.

• Prepare and review key quality system documents, including SOPs, specifications, batch manufacturing records, and periodic product review reports.
• Gather and analyse quality system data to identify trends and insights.
• Support the effective operation of site by:
• Assist in the planning and execution of internal and external audits.
• Stay up to date with GMP standards, regulatory requirements, and industry amendments.
• Ensure personal training records remain current and compliant.
• Promote and contribute to a culture of continuous improvement.
• Step in as a delegate for the QA Manager as needed.

Skills:

• Degree in a relevant field such as Science, Pharmacy, Biotechnology, or a related discipline.
• Minimum of 2-3 years of experience in Quality Assurance within the pharmaceutical or medical device industry.
• Strong knowledge of GMP regulations and compliance requirements.

Apply directly now, or send your updated CV to Ben Byrne at bbyrne@i-pharmconsulting.com OR (04) 21776703

ABOUT i-PHARM CONSULTING

i-Pharm Consulting is a specialist Recruitment Company servicing the global Life Sciences industry. We provide both permanent and contract staff to a wide range of Pharmaceutical, Medical Device, Biotechnology and Contract Research Organisations (CROs). i-Pharm has specific expertise in Clinical Research, Medical Affairs, Regulatory Affairs, Pharmacovigilance, Quality Assurance and Bioinformatics.