GMP Project Officer
Casual Role | Immediate Start | Brisbane
About the Opportunity Join a Brisbane-based life sciences organisation operating within a GMP-regulated biologics manufacturing environment. Supporting advanced bioprocessing operations, this role offers strong exposure to equipment validation, qualification, and continuous improvement initiatives across a technically advanced facility.
This is an excellent opportunity for someone looking to deepen their experience in bioreactor systems, GMP validation, and equipment lifecycle management.
About the Role Working closely with Validation, Engineering, Manufacturing, and Quality teams, you will support the delivery of equipment and process validation activities across the site.
Key responsibilities include: - Supporting qualification and validation of bioprocess equipment, including bioreactors and associated systems
- Authoring and executing IQ/OQ/PQ protocols and validation documentation
- Assisting with commissioning and implementation of new manufacturing equipment
- Maintaining and updating GMP documentation (SOPs, protocols, risk assessments, change controls)
- Supporting deviations, CAPAs, and change management related to validation activities
- Collaborating with cross-functional teams to ensure GMP compliance and project delivery
About You - Degree in Biotechnology, Bioprocess Engineering, or related discipline
- 2–5 years’ experience in GMP biologics or pharmaceutical manufacturing
- Hands-on experience in equipment qualification/validation (IQ/OQ/PQ)
- Exposure to bioreactors, upstream/downstream processing, or process equipment
- Strong understanding of GMP, validation lifecycle, and quality systems
- Confident working in cross-functional, project-driven environments
Apply A strong opportunity to build specialised experience in bioprocess equipment validation and GMP manufacturing within a collaborative and technically advanced setting. Apply now or contact Ruby on ruby@keselect.com for a confidential discussion.
