Back to Job SearchA leading organisation in the pharmaceutical industry is seeking a Cleaning Validation Engineer to join their team in the Walloon region, Belgium. In this role, you will leverage your expertise in cleaning validation to ensure patient safety, regulatory compliance, and sustainable processes. You will support both routine operations and project activities, aligning with the company's unified mindset.
KEY DUTIES AND RESPONSIBILITIES:
Your duties as the Cleaning Validation Engineer will be varied however the key duties and responsibilities are as follows:
1. As the Cleaning Validation Engineer, you will contribute to the definition and continuous improvement of robust, science- and risk-based cleaning strategies.
2. As the Cleaning Validation Engineer, you will support the development and optimisation of cleaning processes and methods.
3. As the Cleaning Validation Engineer, you will author, review, and support approval of Cleaning Validation documentation, ensuring compliance with current GMP expectations and regulatory guidelines.
4. As the Cleaning Validation Engineer, you will drive harmonisation and standardisation of practices across Business Units, facilitating knowledge sharing and lessons learned.
ROLE REQUIREMENTS:
To be successful in your application to this exciting role as the Consultant Cleaning Validation Engineer we are looking to identify the following on your profile and past history:
1. Relevant degree in a scientific or engineering discipline.
2. Proven industry experience in cleaning validation within a regulated environment.
3. A working knowledge and practical experience with GMP, regulatory guidelines, and cleaning validation processes.
Key Words:
Cleaning Validation Engineer / Cleaning Validation / GMP / Pharmaceutical / Regulatory Compliance / Cleaning Processes / Validation Documentation / Risk-Based Strategies / Quality Oversight / Continuous Improvement / MACO / PDE / HBEL / Health-Based Exposure Limits / Cleaning Validation Protocols / Cleaning Validation Reports / Deviation Management / CAPA / Root Cause Analysis / Inspection Readiness / Audit Readiness / Data Integrity / Qualification & Validation (Q&V) / Process Optimisation / Equipment Cleaning / Worst-Case Approach / Bracketing / Grouping Strategies / Cross-Functional Collaboration / SOP Development / Regulatory Inspections / Quality Management Systems (QMS) / Knowledge Sharing / Technical Expertise / Process Validation / Cleaning Strategy Development / Contamination Control / Pharmaceutical Manufacturing / Validation Lifecycle / Risk Assessment / Compliance Audits / Continuous Improvement Culture / Operational Excellence / Validation Governance / Digitalisation in Validation / Quality Assurance / Investigation Support
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the Life Science sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career.
