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Quality control systems specialist

Melbourne
Healthcare Professionals Group
Quality
Posted: 7 June
Offer description

Benefits
* Competitive salary package.
* Immediate start opportunity within a leading global pharmaceutical.
* Exposure to quality systems, compliance, and technical operations.
* Collaborative team environment with strong opportunities for professional development.
About the Company

Join a global pharmaceutical powerhouse recognised for its commitment to quality, innovation, and operational excellence. Supporting the development and supply of products that positively impact patient outcomes, the organisation operates within a highly regulated environment where quality and compliance are central to business success. With a strong culture of continuous improvement and collaboration, this is an opportunity to contribute to a quality-focused team supporting critical operations across a complex manufacturing and laboratory environment.

About the Opportunity

An opportunity exists for a Quality Control Systems Specialist to join a high-performing quality function supporting compliance, documentation, and quality system activities within a regulated environment. Working closely with operational and technical teams, you will play a key role in maintaining quality systems, supporting documentation processes, managing quality records, and contributing to investigations and change initiatives. This role offers a combination of technical, compliance, and project-based responsibilities, making it ideal for someone who enjoys working across multiple quality disciplines.

Duties
* Manage controlled documentation activities, ensuring procedures, specifications, and technical records remain current and compliant.
* Support quality system processes including investigations, deviations, change controls, and corrective actions.
* Coordinate quality activities associated with material qualification, laboratory processes, and operational systems.
* Assist with technical documentation, report preparation, and compliance-related records management.
* Contribute to audit readiness activities by maintaining robust documentation and supporting inspection preparation.
Skills and Experience
* Degree qualification in Chemistry, Pharmaceutical Sciences, Life Sciences, or a related scientific discipline.
* Previous experience within a Quality Control, Quality Assurance, or regulated laboratory environment.
* Experience working with quality systems, controlled documentation, and compliance frameworks.
* Exposure to material qualification activities, specification management, or laboratory operations is highly regarded.
* Experience using electronic quality management or laboratory information systems is advantageous.
* Strong technical writing, documentation, and report preparation skills.
Culture

Join a collaborative and quality-driven organisation that values accountability, continuous improvement, and scientific excellence. Employees are encouraged to contribute ideas, challenge existing processes, and play an active role in maintaining high standards of quality and compliance across the business.

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