We are partnering with a leading global pharmaceutical manufacturer to recruit a Validation Operations Associate on a 6 month-fixed-term contract to support site-based validation activities.
This role offers a unique opportunity for a technically strong validation professional to step into a high-impact, standalone position with strong cross-functional exposure.
6-month fixed-term contract in regional NSW
WHV candidates are welcome to apply
Apply your hands on validation experience in the pharmaceutical industry
About the Role
As the Validation Operations Associate, you will take ownership of process, cleaning, and media fill validation activities, ensuring compliance with GMP standards across the site.
Working within a matrix workplace, you will collaborate closely with teams across Manufacturing, Quality, Engineering, and Technical Operations.
This position is ideal for someone with hands-on validation experience in a GMP manufacturing environment who is confident working autonomously and engaging across departments.
Key Responsibilities
Develop, execute, and report on process validation programs,



cleaning validation activities and media fill requirements.
Partner with site teams to support process improvements and validation initiatives
Support new product introductions and ongoing manufacturing activities
Assist with deviations, investigations, and CAPA management
Prepare and review validation documentation and protocol & SOPs and batch records
Provide technical support across Manufacturing and Quality functions
Skills and Qualifications
To be successful in this role, you will have:
a Degree in Science, Engineering, or a related discipline
Proven experience in process validation within a manufacturing environment
Strong experience in validation documentation and reporting
Background working in a GMP-regulated pharmaceutical or related industry
Ability to work independently in a standalone role
Strong communication skills and the ability to engage cross-functionally
This a full-time on-site rolewith flexibility to start any time between 7:00am – 9:00am.
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📌 Validation Associate ( Contract Role) (New South Wales)
🏢 On Q Recruitment
📍 New South Wales