Walker Cole International is currently supporting a leading pharmaceutical manufacturer in their search for a Senior Validation Officer to join their Quality Assurance function at their site based in West Yorkshire.
The company specialises in the manufacture of patient-centric medicines and is committed to the development and global supply of novel-dose pharmaceuticals. This role offers the opportunity to play a key part in validation projects and continuous improvement initiatives across manufacturing and quality operations.
Key Responsibilities:
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Lead and execute validation activities in line with GMP regulations and company SOPs.
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Author and review validation protocols, reports, and risk assessments (including FMEA and root cause analysis).
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Act as deputy to the Validation Manager and provide mentorship to junior validation team members.
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Support the tech transfer of new products, ensuring all process and cleaning validation requirements are met.
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Monitor and report on key Quality metrics, and contribute to regulatory submissions and audit readiness.
The successful candidate will have:
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A degree (or equivalent experience) in a scientific or engineering discipline.
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Significant experience in a GMP-regulated pharmaceutical manufacturing environment.
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Proven track record of authoring and executing validation protocols.
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Familiarity with quality systems, risk assessment methodologies, and regulatory expectations for validation.
This is an excellent opportunity to step into a supervisory role and contribute to the development and validation of essential pharmaceutical products.