Validation Engineer

This role offers the chance to work in a dynamic and innovative environment where your technical expertise will drive meaningful impact.

• Manage and execute projects that ensure safety, regulatory compliance, operational requirements, and business objectives.
• Develop structured project plans to improve efficiency, equipment utilization, waste reduction, and cost management.
• Provide technical support by identifying and solving process deficiencies, modifications, and equipment failures.
• Challenge and improve existing processes by developing new and innovative approaches.
• Work with cross-functional teams to ensure compliance with GMP/ISO regulations and address product design changes.
• Lead investigations into non-conformance issues, including root cause analysis and corrective actions.
• Manage NCR/CAPA files from initiation to final approval.
• Support manufacturing by troubleshooting equipment and ensuring accurate documentation.
• Participate in GMP audits and maintain communication with end users and machine manufacturers.
• Ensure compliance with J&J safety standards and promote a safe working environment.
• experience

• skills
• Bachelor's degree in Engineering.
• 2 – 4 years in process or maintenance engineering, preferably within the medical devices industry
• Project management experience and training.
• Strong computer skills, including MS Office, MS Project, PowerPoint, Excel, Word, Outlook, Minitab.
• Experience in manufacturing standards development and equipment troubleshooting.
• Project management skills and training.
• Experience of knowledge in short and long term project management.
• Basic computer skills and use of software application(s). Strong computer background
• qualifications

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