Manufacturing Operator

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

Vaxxas is seeking motivated and detail-oriented casual and full-time Manufacturing 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.

About the Role

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

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 develop foundational manufacturing skills, including operation of equipment, cleanroom practices, documentation standards, and Good Manufacturing Practice (GMP) requirements.

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.

Important information:

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.

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.

Key Responsibilities

• Manufacture and prepare in-process and finished products in accordance with approved procedures and work instructions.
• Operate manufacturing equipment and prepare materials, equipment and excipient solutions required for production activities.
• Follow Standard Operating Procedures (SOPs), batch records and quality requirements with a high level of accuracy and attention to detail.
• 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.
• Conduct routine cleaning and maintenance of cleanrooms, laboratories and manufacturing equipment.
• Complete production, quality and batch documentation in accordance with Good Documentation Practice (GDP) and GMP requirements.
• Collect and handle environmental monitoring and quality control samples.
• Maintain cleanliness, safety and quality standards, escalating production, equipment or quality issues as required.
• Support inventory management, validation, qualification and continuous improvement activities.
• Collaborate with Manufacturing, Quality and R&D teams to support process development and technology transfer activities.

Qualifications (Desirable)

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

Skills & Attributes

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

Why Join Vaxxas?

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

• Gain valuable exposure to regulated manufacturing and product development environments (GMP/QMS).
• Work in a supportive team environment that fosters learning and growth.
• Build practical, transferable skills and a strong foundation for a career in biotech, pharma, or technical operations.

This role is NOT suitable for candidates who:

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

To be considered, please submit your Resume and a cover letter (outlining your core capability for the role, demonstrated experience of how you have delivered outcomes and why this role is of interest) by selecting the “apply for this job” function. You will be contacted directly if your application is successful.