Job Title

Social network you want to login/join with: Compliance & Validation Manager, Nottinghamcol-narrow-left Client:Reckitt Location:Nottingham, United Kingdom Job Category:Other - EU work permit required:Yes col-narrow-right Job Reference:71cf7c92acf8 Job Views:6 Posted:17.06.2025 Expiry Date:01.08.2025 col-wide Job Description:Compliance & Validation Manager City: Nottingham About Reckitt Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose is to protect, heal, and nurture for a cleaner, healthier world. Join us in our mission to make access to quality hygiene, wellness, and nourishment a right, not a privilege. Role OverviewAs a Qualified Person supporting batch certification and release activities, you'll work closely with Project Engineers and the Technical team to oversee validation activities, ensuring new equipment and process changes meet quality standards. You'll collaborate with Third Party and Reckitt manufacturing sites to resolve quality issues and support product supply to Nottingham. The role involves proactive risk management and continuous improvement. Your ResponsibilitiesBatch release and certification of finished products at Nottingham. Maintain GMP compliance for all factory activities. Provide quality input and sign-off on validation activities, including facilities, equipment, NPD/EPD, and product transfers. Implement NPD/EPD with clear risk management. Coordinate with third-party and Reckitt manufacturing sites on quality issues and changes. Identify and communicate non-compliance and risks to supply management. Support regulatory audits to maintain manufacturing authorizations and export agreements. Display performance indicators and risks to management. Provide technical support for investigations and quality issues. Qualifications & ExperienceEligible to act as a Qualified Person in the UK. Understanding of manufacturing operations and quality management systems. Knowledge of pharmaceutical manufacturing regulations in Europe. Proven track record in manufacturing environments. Experience in pharmaceutical manufacturing of solid dosage forms. Validation, training, and auditing experience. Skills for SuccessQualified Person, Pharmaceutical, Manufacturing Operations, Quality Management Systems. What We OfferInclusive culture, wellbeing benefits, share plans, incentives, and career development opportunities. Equality StatementWe hire for potential and value diversity. All qualified applicants will receive consideration without discrimination based on age, disability, ethnicity, gender, and other protected characteristics.#J-18808-Ljbffr