Cleaning Validation Specialist

il y a 4 semaines


Geel, Belgique Panda International Temps plein

About the Role: We are seeking an experienced Cleaning Validation Specialist to join our client's Manufacturing Science and Technology (MSAT) team. This role focuses on cleaning validation in pharmaceutical manufacturing, ensuring processes meet strict quality and regulatory standards. You will manage validation activities, documentation, audits, and support the introduction of new products and equipment, contributing to compliance and operational excellence. Key Responsibilities: Prepare and update cleaning validation documentation, including protocols, reports, and studies. Gatekeep proposed changes and prioritize cleaning validation projects. Support audits and ensure timely responses to findings. Facilitate the introduction of New Product Introductions (NPI) and new equipment in the validation program. Report incidents, deviations, and propose solutions to improve compliance. Collaborate with cross-functional teams, including manufacturing, quality, and engineering. Key Competencies: Strong expertise in API manufacturing processes and cleaning validation. Solid understanding of validation principles and statistical methods. Knowledge of Quality & Compliance/regulatory requirements (GMP) in cleaning validation. Project management, planning, organization, and coordination skills. Ability to manage complexity, deadlines, and competing priorities. Excellent communication and interpersonal skills, able to interact at different organizational levels. Familiarity with systems such as eLIMS, truVAULT, COMET, PRX, CRB, SAP, PASx, Minitab, CPV Automation (preferred). Requirements: 2–4 years of relevant work experience in pharmaceutical manufacturing or validation. Practical's: Location: Geel, Belgium Duration: 12+ months Start Date: ASAP Work Model: Full-time, On-site


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