Are you passionate about quality, documentation and continuous improvement? Do you thrive in a fast-paced manufacturing environment where accuracy and compliance matter?
If so, you'll fit right in at Mayne Pharma. What's in it for you? You'll help us achieve our mission of delivering better, safer and more accessible medicines.
At Mayne Pharma, the results speak for themselves.
About Mayne Pharma
Mayne Pharma is a global pharmaceutical company offering end-to-end pharmaceutical development and manufacturing to customers around the world. Our heritage makes us one of the most well-known and respected pharmaceuticals companies in Australia.
Mayne Pharma Australia are passionate about bringing globally valued pharmaceuticals to Australian patients and consumers. Our values of Passion, Integrity, Accountability, Creativity, Empowerment and Agility are the foundation for everything we do.
Why Join Us?
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Attractive remuneration packages
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Exclusive Health Insurance Benefits
Financial Flexibility -
Well-being Programs
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Professional Development
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Mayne Perks: Enjoy exclusive discounts and savings
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Community Service
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Recognition and Team Events
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Health and Wellness
Here’s where you come in
Are you someone who enjoys creating order, improving processes and ensuring documentation is accurate and compliant? Do you have experience in a regulated manufacturing environment and want to broaden your exposure to quality systems?
If so, you'll join a collaborative and fast-paced Production team where you'll play a critical role in supporting manufacturing excellence through effective document control and quality system support. You'll work closely with Production, Quality Assurance and Subject Matter Experts to ensure documentation remains current, compliant and audit ready while contributing to continuous improvement initiatives across the site.
Your responsibilities, at a glance, will include
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Review, update and maintain production documentation including Standard Operating Procedures (SOPs), Work Instructions (WIs), Master Batch Records and other controlled documents.
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Ensure documentation reviews and updates are completed accurately and within required timeframes.
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Partner with Production, QA and Subject Matter Experts to improve and maintain manufacturing documentation.
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Support Quality Management System (QMS) activities including deviations, non-conformances, CAPAs, Change Controls and investigations.
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Assist with internal and external audit preparation, responses and follow-up activities.
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Support investigations into quality events and assist with implementing effective corrective and preventive actions.
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Develop and update documentation and training materials to support quality improvements.
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Provide documentation support across Production and other departments as required.
Contribute to continuous improvement initiatives that enhance compliance, efficiency and operational performance. -
Perform other duties appropriate to the position as required.
You will have demonstrated experience or have an understanding of:
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Documentation Management: Reviewing, maintaining and improving controlled documentation including SOPs, Work Instructions, Master Batch Records and associated GMP records.
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Quality Systems: Supporting deviations, CAPAs, Change Controls, investigations and other Quality Management System processes.
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Regulatory Compliance: Working within GMP and regulated manufacturing environments while maintaining accurate, audit-ready documentation.
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Collaboration: Building strong working relationships with Production, QA and cross-functional stakeholders to deliver documentation improvements and quality outcomes.
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Continuous Improvement: Identifying opportunities to improve documentation, processes and compliance while supporting operational excellence.
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Computer Skills: Proficiency in Microsoft Office applications including Word, Excel and Outlook.
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Experience within the pharmaceutical, food, cosmetic or other regulated manufacturing industries will be highly regarded.
Additionally experience working within and enjoying the challenge of a high throughput laboratory will be well regarded.
You need to tick these boxes
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A tertiary qualification in Science, Engineering or a related technical discipline, or equivalent industry experience.
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Experience within the pharmaceutical, food, cosmetic or other regulated manufacturing industry.
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Experience supporting documentation, quality systems or manufacturing operations in a regulated environment.
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Strong organisational, communication and time management skills.
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The ability to manage competing priorities while maintaining high levels of accuracy and compliance.
Ready to become part of the Mayne Pharma story?.
How To Apply - Click the APPLY NOW button
