Job Description
Process Validation Specialist (Pharmaceutical Manufacturing)
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About the Company & Role: Join a Leading Veterinary Pharmaceutical Company who specialise in the development and manufacturing of veterinary medicines. This is your chance to be part of a team committed to excellence and innovation.
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An exciting opportunity is available for a Process Validation Specialist to join their Rutherford manufacturing facility on an initial 4-month contract. Working within the Validation team, you will support process validation, cleaning validation and media fill activities while ensuring compliance with GMP requirements.
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This is a documentation-focused role suited to candidates with experience authoring validation protocols and reports, analysing validation data, reviewing batch documentation and collaborating with Quality and Production teams within a regulated manufacturing setting.
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Duties:
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Author and review process validation protocols and reports
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Support process validation, cleaning validation and media fill activities
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Analyse validation data and prepare technical reports
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Review batch and manufacturing documentation
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Ensure validation protocols are executed in accordance with requirements
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Coordinate sample collection and validation activities
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Liaise with Production teams regarding validation planning and execution
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Liaise with Quality teams to support GMP compliance and document approval
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Support new product introduction activities
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Assist with validation‐related deviations, investigations and CAPAs
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Support process improvement initiatives and manufacturing operations as required
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Skills & Experience:
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Bachelor's Degree in Science, Chemical Engineering, Industrial Engineering or a related discipline
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3+ years' experience within pharmaceutical, biopharmaceutical, consumer healthcare or cosmetics manufacturing environments
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Direct validation experience within a regulated GMP environment
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Experience authoring validation protocols and validation reports
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Strong data analysis and technical documentation skills
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Experience reviewing batch documentation and manufacturing records
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Understanding of pharmaceutical quality systems and GMP requirements
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Experience with Minitab, SAP, ETS, Viva document control systems - highly regarded
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Experience with synthetic chemical manufacturing processes - highly regarded
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Strong communication and stakeholder engagement skills
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Ability to work autonomously and manage multiple priorities
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Culture & Benefits:
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Free on-site parking for your convenience
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Be part of a collaborative and experienced technical team
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Work closely with Validation, Production and Quality professionals
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Gain exposure to a globally recognised veterinary pharmaceutical manufacturer
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Supportive team environment with strong technical leadership
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Please Note:
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A police check and pre-employment medical (including drug and alcohol screening) are required prior to commencement. These will be organised by the company.
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📌 Process Validation Specialist (Pharmaceutical Manufacturing) (New South Wales)
🏢 Evolve Scientific
📍 New South Wales