Southern RNA
Services / Develop & Manufacture

Analytical & Process Development

Southern RNA is Australia’s leader in mRNA development and manufacturing. We empower biotech innovators with high-quality nucleic acids and scalable GMP platforms, accelerating therapies from research to impact.
KEY RESPONSIBILITIES

Design, execute, and analyse experiments related to RNA construct development and optimisation

Develop and refine protocols for in vitro transcription, purification, and analytical testing

Collaborate with process development, manufacturing, and quality teams to support scale-up and GMP-aligned workflows

Maintain accurate and detailed laboratory records and documentation in compliance with quality systems

Contribute to problem-solving, process improvement, and knowledge sharing within the R&D team

EXPERIENCE & SKILLS

Degree in Molecular Biology, Biochemistry, Biotechnology, or a related discipline

Hands-on experience with RNA, plasmid DNA, or nucleic acid-based workflows

Familiarity with molecular biology techniques such as PCR, cloning, RNA handling, and transfection assays

Strong analytical skills, attention to detail, and ability to interpret experimental data

Excellent communication, teamwork, and organisational skills in a laboratory setting

Experience working under GMP or quality-regulated environments is an advantage

APPLICATION PROCESS
To apply, please submit your CV and a brief cover letter highlighting your relevant experience and interest in RNA science. Shortlisted candidates will be invited to an initial interview, followed by a technical assessment and final discussion with the R&D leadership team.

We are committed to creating an inclusive and supportive workplace and encourage applications from all qualified candidates.

    FAQS

    Your Questions Answered

    Our FAQ section addresses the most common technical and compliance queries, providing clarity on our capabilities, processes, and quality systems.

    Yes, our facilities produce GMP-aligned and clinical-grade mRNA and plasmid DNA suitable for early-phase trials.

    We follow GMP-aligned processes, robust documentation, and quality oversight to meet regulatory expectations and support submissions.

    We offer flexible production from milligram-scale research material to multi-gram clinical-grade batches.

    Yes, our in-house analytical team supports identity, purity, impurity profiling, and stability testing across all projects.

    Absolutely. Our team develops reproducible processes for smooth transition from research-scale to GMP-aligned clinical production.