Process Development Scientist

Job Description

Get AI-powered advice on this job and more exclusive features. Direct message the job poster from KE Select - Scientific & Medical Recruitment Specialists Head of Client Partnerships | Empowering companies to build high-impact teams | Strategically aligning top-tier talent with exceptional career… Process Development Scientist – Upstream About VVMF Viral Vector Manufacturing Facility (VVMF) has exclusively partnered with KE Select Scientific & Medical Recruitment Specialists to support their recruitment strategy and growth. VVMF is the first commercial manufacturing facility of its kind in Australia. Based at the Westmead Health Precinct in Westmead, NSW, VVMF are uniquely integrated in the largest health, education, research, and innovation precinct in the country. VVMF is set to become a leading Contract Development and Manufacturing Organisation (CDMO) in Asia-Pacific, producing clinical and commercial grade viral vectors for advanced therapeutic applications. VVMF is building a values-based organisation that is committed to equality, diversity, and inclusion. They aim to deliver an outstanding product and are committed to excellence in service and experience for everyone associated with their facility. The Opportunity The opportunity is available for Process Development Scientist - Upstream to join the VVMF facility. Reporting directly to the Hiring Manager, you will be responsible for the development of cutting-edge gene therapy vectors. As a Scientist - Upstream, you will play a crucial role in the advancement of adeno-associated virus (AAV) and lentiviral (LV) manufacturing processes, supporting transformative therapies for patients in need. Key Responsibilities: Upstream Production: Assist in the development and optimization of upstream production processes, collaborating with section leads to execute experiments and perform essential quality control assays. Technology Transfer: Aid in the smooth technology transfer of processes to VVMF’s GMP cleanroom facility, ensuring adherence to regulatory standards and supporting production staff during this critical transition. Quality Control Assays: Engage in the design and execution of quality control assays specific to gene therapy vectors; source reagents and support experiments for assay development. Laboratory Operations: Oversee day-to-day laboratory operations, including ordering reagents, equipment maintenance, and troubleshooting, while supporting cross-functional teams in investigations and improvements. What We’re Looking For: Essential Qualifications: Science degree or equivalent experience in pharmaceutical, biological, or health sciences. Proven experience in cell and tissue culture of both adherent and suspension mammalian cells. Proficient in technical assays, including qPCR, Western blotting, flow cytometry, ELISA, and chromatography. Knowledgeable about Good Manufacturing Practices (cGMP) and relevant clinical trial frameworks. Personal Attributes: Excellent organizational and communication skills, able to engage diverse audiences with ease. A proactive problem solver, innovative thinker, and dependable team player with a positive, "can do" attitude. Exceptional attention to detail and the ability to manage multiple tasks effectively. Background in viral vector manufacturing and analytical techniques. Experience in agile project management. To be considered for this current opportunity, or any other opportunities within the Viral Vector Manufacturing Facility (VVMF), please send your CV to our regularly attended dedicated VVMF careers inbox: For any confidential discussion, please contact Yash (0401 271 481) Seniority level Mid-Senior level Employment type Full-time Job function Manufacturing and Production Industries Manufacturing and Biotechnology Research #J-18808-Ljbffr