Signet Jewelers is hiring a Project Engineer to lead site support for the implementation of eDHR (electronic Device History Record) software. This is a 2-year project focused on deploying and integrating systems across production lines to meet stringent operational and regulatory requirements.

What You'll Do

Lead the deployment and integration of eDHR systems across production lines or healthcare facilities.
Ensure systems are configured to meet operational, regulatory, and quality requirements.
Collaborate with IT and software vendors to ensure seamless data flow and system interoperability.
Develop detailed project plans, timelines, and resource allocations.
Coordinate cross-functional teams including Quality, Operations, IT, and external vendors.
Track milestones and ensure timely delivery of project phases (design, testing, go-live).
Ensure eDHR systems comply with industry regulations.
Maintain accurate documentation of system configurations, validations, and change controls.
Support audits by providing traceable and validated digital records.
Develop training materials and conduct sessions for end-users.
Provide ongoing support and guidance to ensure effective system adoption.
Monitor user feedback and implement system enhancements as needed.
Collaborate with QA teams to validate system functionality and data integrity.
Conduct performance testing and ensure the system meets quality standards.
Support UAT (User Acceptance Testing) and resolve any identified issues.

What We're Looking For

Bachelor’s degree in engineering, Computer Science, Information Technology, or related field.
3–5 years of experience in medical device manufacturing, MES implementation, or digitalization projects.
Hands-on experience with Apriso configuration, deployment, and support.
Experience with MES systems, preferably Dassault Systèmes Apriso.
Familiarity with eDHR systems, digital manufacturing, and system integration.
Understanding of database systems and data flow.
Proficiency in system validation and quality assurance testing.
Proven ability to lead cross-functional teams (Quality, IT, Operations, Vendors).
Strong skills in project planning, resource allocation, and timeline management.
Experience managing digital transformation or IT implementation projects in regulated environments.
Familiarity with medical device regulations in Malaysia and globally (e.g., MDA, FDA, EU MDR).
Experience in documentation, change control, and audit support.
Excellent communication skills for stakeholder engagement and user training.
Ability to develop training materials and conduct end-user sessions.
Strong analytical and problem-solving skills to address system feedback and enhancements.
Experience working in multinational environments or with global teams.