gxp quality

Our client, a leading pharmaceutical manufacturing company based in Brisbane's western suburbs, is seeking a Documentation Officer for a casual ongoing role in a predominantly office-based setting. The successful candidate will work Monday to Friday with a focus on quality-driven documentation control and regulatory compliance.Ideal applicants will hold a...

CAI is seeking a hands-on CSV Specialist to join a cutting-edge advanced therapeutics facility in Sydney, Australia. This full-time role focuses on validation activities within GxP environments, delivering compliant, high-integrity systems and processes. You will lead IQ/OQ/PQ across ERP, LIMS, QMS, and equipment software, collaborate with IT, QC, and...

We are looking for a Quality Assurance Engineer to join our team on a 12‑month contract. The role is responsible for providing Quality Assurance oversight and support for commissioning, qualification, validation, technology transfer, process lifecycle management, capital projects, vendor qualification, and operational quality activities. The incumbent will...

Melbourne, Australia | Posted on 07/08/2026 We are looking for a Quality Assurance Engineer to join our team on a12-month contract. The Quality Assurance Engineer is responsible forproviding Quality Assurance oversight and support for commissioning,qualification, validation, technology transfer, process lifecycle management,capital projects, vendor...

CAI is seeking a hands-on CSV Specialist to join a cutting-edge advanced therapeutics facility in Sydney, Australia. This full-time role focuses on validation activities within GxP environments, delivering compliant, high-integrity systems and processes.You will lead IQ/OQ/PQ across ERP, LIMS, QMS, and equipment software, collaborate with IT, QC, and...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

1. Planning and hosting of client audits and/or regulatory inspections of Novotech. 2. Perform audits of investigator sites, vendors, Trial Master Files, internal processes and systems. 3. Ensure that audit results are formally recorded and reported in a timely manner and that corrective / preventive actions are implemented effectively. 4. Participate in the...

We are looking for a Quality Assurance Engineer to join our team on a 12‑month contract. The role is responsible for providing Quality Assurance oversight and support for commissioning, qualification, validation, technology transfer, process lifecycle management, capital projects, vendor qualification, and operational quality activities. The incumbent will...

Quality Assurance and CSV Associate – Pharmaceutical Industry JAG Process Solutions Pty Ltd (JAG PS) is a unique process automation solutions company that has been at the forefront of innovation and technology in Europe and continues to expand its footprint in the Australian market. Your responsibilities Ensure full compliance with cGMP requirements as...

Senior Associate – Global Regulatory Affairs & QualitySenior Associate – Global Regulatory Affairs & QualityGet AI-powered advice on this job and more exclusive features.This range is provided by Proclinical Staffing. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.Base pay rangeA$115,000.00/yr -...

1. Planning and hosting of client audits and/or regulatory inspections of Novotech.2. Perform audits of investigator sites, vendors, Trial Master Files, internal processes and systems.3. Ensure that audit results are formally recorded and reported in a timely manner and that corrective / preventive actions are implemented effectively.4. Participate in the...

Medicines Development for Global Health is seeking a senior Quality leader in Melbourne to oversee the MDGH Quality System across GxP activities, with emphasis on GMP and GCP. You will partner with CMC, Regulatory and Clinical teams, vendors and consultants to ensure compliance and drive quality across development activities. You will lead internal/external...

For the past 25 years, ProPharma has improved the health and wellness of patients by providing advice and expertise that empowers biotech, med device, and pharmaceutical organizations of all sizes to confidently advance scientific breakthroughs and introduce new therapies. ProPharma partners with its clients through an advise-build-operate model across the...

GLP Vendor Oversight and QA LeadThe integrity of nonclinical data depends on more than what happens inside a company's walls. Much of the critical work in GLP-regulated research — safety studies, toxicology, analytical testing — is carried out by external laboratories and CROs. When that network of partners operates to the highest quality standards, the...

We are looking for a Quality Assurance Engineer to join our team on a 12-month contract. The Quality Assurance Engineer is responsible for providing Quality Assurance oversight and support for commissioning, qualification, validation, technology transfer, process lifecycle management, capital projects, vendor qualification, and operational quality...

Outstanding career opportunity in pharmaceutical quality Medicines Development for Global Health – Southbank VIC As the responsible person for Quality at MDGH, you will manage the MDGH Quality System across regulated activities (GxP), with particular focus on Good Manufacturing Practice (GMP) and Good Clinical Practice (GCP). Working closely with our CMC,...

CAI Overview Are You Ready? CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest...

Commissioning Qualification Validation Engineer Brisbane, Australia | Posted on 06/03/2026 PSC Biotech provides the life sciences with essential services to ensure that health care products are developed, manufactured, and distributed to the highest standards, in compliance with all applicable regulatory requirements. Our goal is to skyrocket our...

Your Role We are looking for a Commissioning, Qualification, and Validation (CQV) Engineer to join our team on a 12-month contract. The CQV Professional will work alongside a talented PSC Biotech team in an exciting, developing, and diverse biotechnology landscape. Commission, qualify, and validate GxP facilities, equipment, and utilities in assigned...

Amentum is a global leader in advanced engineering and innovative technology solutions,trusted by the United States and its allies to address their most significant and complex challenges in science, security and sustainability. Our people apply undaunted curiosity, re-lentless ambition and boundless imagination to challenge convention and drive progress.Our...