About the Role Our Client, a pharmaceutical manufacturing company based in the Brisbane region, is seeking a Quality Systems Specialist for a contract position through to the end of the year. This role is predominantly desk‑based and requires a strong attention to detail, sound judgement, and prior experience working within a regulated environment. As a Quality Systems Specialist, you will support the coordination and maintenance of the Quality Management System to ensure compliance with GxP, regulatory, and internal quality requirements across impacted sites. This role is suited to someone with previous pharmaceutical or regulated industry experience who is comfortable working independently and engaging with multiple stakeholders. NOTE: Applicants will be required to undertake a full medical assessment, drug screening and police check to be eligible for this role. Please note that the site is not easily accessible by public transport, therefore access to a reliable vehicle is essential to travel to and from work. The successful candidate will be responsible for, but not limited to:Coordinating compliance activities to ensure adherence to GxP and regulatory requirementsReviewing, updating, maintaining, and supporting training related to quality master documentsCompiling and completing documentation to support quality system changes and related change requestsTracking Quality Management System performance, including KPIs and escalation reportingSupporting inspection and audit readiness for regional sites and quality system processesLiaising with local and global stakeholders to support system maintenance and quality changesManaging quality‑related projects through to successful completionSupporting continuous improvement initiatives within the Quality Systems functionEnsuring all activities comply with GxP, legal, and ethical standards Skills & Experience The successful candidate must have:Degree‑level qualification in a scientific discipline or related fieldExperience within the pharmaceutical industry, biotech, medical devices, or another regulated manufacturing environmentWorking knowledge of GMP / GxP requirementsExperience working with Quality Systems and controlled documentationStrong attention to detail and the ability to manage competing prioritiesExcellent written and verbal communication skillsConfidence working independently and engaging with cross‑functional and global stakeholders Apply! If you think this could be the role for you, please apply now! Submit a cover letter and a detailed resume in WORD format (PDFs may not be processed). If you have any questions, please contact Raine on 07 3175 0680.With over 90 years' combined experience, NES Fircroft (NES) is proud to be the world's leading engineering staffing provider spanning the Oil & Gas, Power & Renewables, Chemicals, Construction & Infrastructure, Life Sciences, Mining and Manufacturing sectors worldwide. With more than 80 offices in 45 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. We offer contractors far more than a traditional recruitment service, supporting with everything from securing visas and work permits, to providing market-leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.