Validation Specialist | Pharmaceutical | Kent | Permanent | up to £55,000 DOE
Are you a Validation Specialist with a passion for cleaning validation, GMP compliance, and equipment qualification? Join a leading pharmaceutical company where your work will directly contribute to safe, high-quality pharmaceutical production.
What You’ll Do:
Execute validation protocols (IQ/OQ/PQ/PV) for equipment, facilities, and processes
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Cleaning validation activities, develop protocols, sampling strategies, set limits, and compile reports
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Perform temperature mapping and requalification of GMP-critical equipment
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Draft and maintain validation documentation, including master plans and SOPs
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Collaborate closely with QA, Engineering, and Production to ensure compliance with minimal disruption
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Support internal and external audits and inspections
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Stay current with regulatory guidelines (Annex 15, ISO 13485, EudraLex Vol 4) and drive process improvements
What You’ll Bring:
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2+ years' validation experience in a GMP-regulated pharmaceutical environment
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Hands-on experience with cleaning validation, including protocol writing and execution.
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Knowledge of Annex 11, Annex 15, ISO 9001, and ISO 13485
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Familiarity with calibration principles, validation lifecycle, and documentation standards
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Strong written and verbal communication skills
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Proficient in Microsoft Word, Excel, and PowerPoint
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Highly organised, detail-oriented, and proactive
Why Apply?
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Join a well-established pharmaceutical company known for quality and innovation
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Greats benefits packages that includes Annual Incentive Plan, Private Medical Insurance and Life Assurance
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Be part of a supportive, collaborative team environment
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Play a key role in high-impact projects that matter
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Benefit from professional development opportunities and a structured career path
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