Job Description

Kick-start your career in biotechnology manufacturing, developing hands-on skills in cleanroom operations, quality systems, and the production of innovative healthcare products.

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Vaxxas is seeking motivated and detail-oriented casual and full-timeManufacturing Operators to join our collaborative production team. This entry-level opportunity is ideal for recent graduates and early-career professionals looking to gain hands-on experience in advanced manufacturing while developing valuable skills in GMP, cleanroom operations and quality systems.

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About the Role

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The Manufacturing Operator plays an important role in supporting the manufacture of sub-assemblies, intermediate products, and finished products within a highly regulated manufacturingenvironment.

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This is a hands-on, entry-level role suited to recent graduates or individuals looking to start a career in combination med-pharma manufacturing. Comprehensive training will be provided to developfoundational manufacturing skills, including operation of equipment, cleanroompractices, documentation standards, and Valuable Manufacturing Practice (GMP)requirements.

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Working as part of a collaborative team, the Manufacturing Operator will contribute to meeting production schedules while maintaining the highest standards of quality, safety and compliance.

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This role is performed within a highly controlled cleanroom manufacturing environment. Employees are required to wear cleanroom garments and personal protective equipment (PPE), follow strict hygiene and contamination-control procedures, and work within regulated manufacturing areas for extended periods.

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As part of the recruitment process, successful candidates will be required to complete a pre-employment medical assessment to ensure they can safely perform the inherent requirements of the role.

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Key Responsibilities

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- Manufacture and prepare in-process and finished products in accordance with approved procedures and work instructions.
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- Operate manufacturing equipment and prepare materials, equipment and excipient solutions required for production activities.
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- Follow Standard Operating Procedures (SOPs), batch records and quality requirements with a high level of accuracy and attention to detail.
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- Work within controlled cleanroom environments (ISO 5, 6, 7 and 8; Grade A, B, C and D), adhering to gowning, contamination-control and aseptic practices.
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- Conduct routine cleaning and maintenance of cleanrooms, laboratories and manufacturing equipment.
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- Complete production, quality and batch documentation in accordance with Good Documentation Practice (GDP) and GMP requirements.
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- Collect and handle environmental monitoring and quality control samples.
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- Maintain cleanliness, safety and quality standards, escalating production, equipment or quality issues as required.
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- Support inventory management, validation, qualification and continuous improvement activities.
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- Collaborate with Manufacturing, Quality and R&D; teams to support process development and technology transfer activities.
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Qualifications (Desirable)

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- Tertiary qualifications (completed or in progress) in Science, Biotechnology, Engineering, Pharmacy, Chemistry, Biological Sciences, Manufacturing, or a related discipline.
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- Previous experience in a manufacturing, laboratory, healthcare, pharmaceutical, biotechnology, or regulated environment.
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- Demonstrated interest in developing a career within advanced manufacturing, pharmaceutical production, biotechnology, or medical devices.
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- Basic computer skills, including Microsoft Office applications.
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Skills & Attributes

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- Strong attention to detail and commitment to quality.
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- Ability to follow procedures and instructions accurately and consistently.
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- Willingness to learn and develop new skills within a regulated manufacturing environment.
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- Comfortable working in cleanroom environments and wearing cleanroom gowning/PPE for extended periods.
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- Effective written communication and documentation skills.
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- Strong organisational skills and ability to manage competing priorities.
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- Ability to work collaboratively as part of a team and proactively raise issues when required.
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- Commitment to workplace safety, quality and compliance standards.
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Why Join Vaxxas?

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Be part of an innovative biotech organisation that provides structured training and development opportunities.

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- Gain valuable exposure to regulated manufacturing and product development environments (GMP/QMS).
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- Work in a supportive team environment that fosters learning and growth.
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- Build practical, transferable skills and a strong foundation for a career in biotech, pharma, or technical operations.
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This role is NOT suitable for candidates who:

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- Are seeking to lead, design, or own scientific experiments or research programs
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- Prefer highly autonomous, exploratory, or innovation-led roles
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- Are looking for a primarily lab-based R&D; or analytical position
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- Are significantly overqualified and seeking immediate senior or specialist responsibilities
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- Are not comfortable working within strict procedures, documentation, and routine tasks
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📌 Manufacturing Operator (Queensland)
🏢 Vaxxas
📍 Queensland