Our vision isExceptional Science, Healthier Lives.The Translational Research Institute (TRI) is a leading Australian medical research, development and translation facility. It is home to a broad range of cutting-edge research into cancer, chronic diseases, mental health conditions, immunology, genetics and more. TRI’s priority is partnering scientific development with clinicians and the MedTech sector to ensure new discoveries progress quickly and improve patient outcomes and commercial return. To this end, TRI is at the interface of science, medicine and industry.In 2022, TRI has been funded to build a new facility adjacent to the Princess Alexandra Hospital / TRI campus which will be known as Translational Manufacturing at TRI (TM@TRI). This facility will be the home of MedTech start-up/scale-up companies to support GMP manufacturing for novel products to support Phase I-III clinical trials.The Translational Manufacturing facility @ Translational Research Institute (TM@TRI) will operate as Australia’s first scale-up multiproduct biomedical cGMP cleanroom facility on demand, for maturing, high-potential, med-tech and biotech start-ups. The Translational Manufacturing facility (TM@TRI) is located at Kent Street, Woolloongabba, QLD 4102 Australia. It is a concrete and steel structure located on Princess Alexandra Hospital grounds. The facility consists of five levels with approximately 7,249m2 floor area of manufacturing, laboratories, warehouse, utility and administration space. The TM@TRI facility consists of co-working office space, PC2 labs, engineering space and 5x dedicated and segregated GMP cleanrooms supported by GMP utilities and infrastructure designed to support both process/product development activities and manufacturing of clinical Phases I, II & III trial product/material(s).Our Benefits include:Opportunity to salary sacrifice superannuation & access to novated leasingFitness Passport (Discounted gym and pool memberships for you and your family members)Flexible Work Options17.5% Annual Leave LoadingAn inclusive and supportive workplace cultureA focus on staff engagement and employee well-beingTraining and development opportunitiesAbout the RoleThe Senior Quality Control Microbiologist is responsible for the oversight and performance of the Environmental Monitoring (EM) program within the cGMP manufacturing facility as well as the release of raw materials/utilities to ensure that both the cleanroom environment and raw materials/utilities and are in suitable biocontamination control.The Senior Quality Control Microbiologist will be instrumental in the development and implementation of core SOPs, workflows and processes relating to the:1.Implementation and ongoing monitoring of the EM program for the cGMP manufacturing facility,2.Outsourcing of raw material, utility and EM sample testing,3.Collation and review of testing results,4.(in house) QC release of raw materials/utilities.The Senior Quality Control Microbiologist will be expected to have a good understanding of facility and laboratory operational matters and possess a high level of communication skills.The Senior Quality Control Microbiologist will act as a liaison between TRI and its tenants to ensure that contamination control is integrated into all aspects of the facility.The Senior QC Microbiologist must ensure open and transparent client communications, utilizing comprehensive risk management strategies and project planning, to ensure a positive customer relationship.This role is offered on a Permanent basis. It will be Full-Time, 38 hours per week.Key Selection CriteriaQualificationsBachelor’s degree in microbiology required.Postgraduate qualifications beneficial.Relevant technical qualifications and/or extensive experience in a cGMP environment.Experience5+ years of experience in a Quality Control Microbiology role.Demonstrated experience in Microbiology program delivery and relationship management.Demonstrated experience in raw material management i.e. raw material testing and release within the biopharmaceutical industryDemonstrated experience supporting and managing cGMP environmental monitoring, testing and reporting programs.Proven track record in accredited GMP environmentsExperience achieving results through other people, people development and management.Experience in leading, enabling and supporting cross-functional teams, developing strategies and goals, and delivering successful outcomes.Developed communication and interpersonal skills, ability to negotiate, consult, manage change, and engage with a diverse range of groups internally and externally.Ability to develop strong and effective working relationships to create innovative solutions.Technical KnowledgeExpertise in microbiological testing techniques, raw material testing and microbial identification.In-depth knowledge of microbiological testing methods and quality control regulations (cGMP, FDA, etc.).Extensive operational knowledge of the cGMP environment.Proficient in data analysis and interpretation, with a strong attention to detailStrong analytical and problem-solving skills, with a proven ability to investigate and resolve complex issues.Ability to act independently and take initiative without direction within established TRI policies and guidelines.To apply for this position, candidates must submit a cover letter addressing the selection criteria and a current resume quotingjob reference 1831.Applications close at 5:00 PM, Monday 9 June 2025. Applications will be reviewed when received and considered for interview prior to the ad closing.TRI encourages applicants from diverse backgrounds to apply.Seniority levelSeniority levelMid-Senior levelEmployment typeEmployment typeFull-timeJob functionJob functionResearch, Analyst, and Information TechnologyIndustriesResearchReferrals increase your chances of interviewing at Translational Research Institute Australia by 2xGet notified about new Quality Control Microbiologist jobs in Brisbane, Queensland, Australia.We’re unlocking community knowledge in a new way. Experts add insights directly into each article, started with the help of AI.
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