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Quality assurance associate

Sydney
i-Pharm Consulting
Quality
Posted: 1 August
Offer description

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This range is provided by i-Pharm Consulting. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.


Base pay range

A$80,000.00/yr - A$90,000.00/yr

Direct message the job poster from i-Pharm Consulting


Recruiting Regulatory Affairs & Quality Assurance Professionals across Australia & New Zealand

Join a Purpose-Driven Organisation Advancing Early-Phase Clinical Research

Are you passionate about quality, detail-oriented, and ready to take the next step in your QA career? This is an exciting opportunity to join a pioneering clinical research organisation at the forefront of early-phase trials. With a dedicated focus on patient safety, innovation, and regulatory excellence, this team is making a meaningful impact on the future of medicine.

As a Quality Associate, you'll play a vital role in supporting clinical study compliance, ensuring adherence to global standards, and contributing to process improvement across the board. This is a dynamic role ideal for someone who thrives in a collaborative environment, enjoys problem-solving, and is eager to grow their career in the clinical research space.

Responsibilities:

* Support the maintenance and improvement of the Quality Management System (QMS).
* Assist in the development and review of SOPs and quality documentation.
* Manage electronic quality systems including Dot Compliance and SiteDocs.
* Support audits, inspections, and CAPA tracking.
* Assist with equipment calibration, validation, and computer system validation (CSV).
* Monitor training, deviations, and quality events via eQMS reporting.
* Support internal audits and vendor qualification activities.
* Contribute to the delivery of quality training for clinical teams.

Skills:

* Bachelor's or advanced degree in life sciences, healthcare, or a related field.
* Experience in a quality-focused role — clinical research or GCP experience is highly regarded but not essential.
* Strong attention to detail and a commitment to quality and compliance.
* Comfortable working with systems and databases (training can be provided).
* Proactive and curious, with a willingness to ask questions, learn, and grow within the role.
* Able to work both independently and collaboratively in a fast-paced, evolving environment.

Apply directly now, or send your updated CV to Ben Byrne at OR 0421776703.


Seniority level

* Seniority level

Associate


Employment type

* Employment type

Full-time


Job function

* Job function

Science and Research
* Industries

Pharmaceutical Manufacturing

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