Process Validation Associate (Pharmaceutical Manufacturing)
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About the Company & Role: Join a Leading Veterinary Pharmaceutical Company who specialize 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 environment.
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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 setting
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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: A police check and pre-employment medical (including drug and alcohol screening) are required prior to commencement. These will be organised by the company.