Role Description - Create, maintain, and audit Bills of Material (BOMs) for fabrication, welding, machining, powder coating, assembly, and other manufacturing processes. - Develop and maintain production routings, labor standards, work centers, and operational sequences within the ERP system. - Ensure ERP data accurately reflects current manufacturing methods and capabilities. - Review engineering releases and implement required ERP updates. - Monitor ERP accuracy and identify discrepancies impacting production, purchasing, inventory, scheduling, or costing. - Support implementation of new products and engineering changes. - Act as the primary liaison between Engineering and Production teams. - Translate engineering designs into executable manufacturing processes. - Verify manufacturability of designs and provide feedback regarding production challenges. - Assist with development and maintenance of work instructions, manufacturing documentation, and process standards. - Participate in engineering review meetings and production planning discussions. - Support Engineering Change Orders (ECOs) and ensure timely implementation on the production floor. - Work directly with supervisors, leads, and operators to validate routing accuracy and labor standards. - Investigate production issues related to BOMs, routings, inventory transactions, and work orders. - Identify process bottlenecks and recommend improvements to increase efficiency. - Monitor production feedback and update ERP data to reflect actual manufacturing practices. - Support scheduling, planning, and capacity analysis activities as needed. - Perform routine audits of BOMs, routings, inventory transactions, and manufacturing data. - Develop and implement process improvements that increase accuracy and reduce administrative burden. - Help establish best practices for ERP utilization across departments. - Support lean manufacturing and continuous improvement initiatives. - Track and report key metrics related to ERP accuracy, routing compliance, and production efficiency. Qualifications - 3+ years of manufacturing, production planning, engineering support, or ERP administration experience. - Strong understanding of Bills of Material (BOMs), routings, work orders, and manufacturing processes. - Experience working within ERP systems. - Proficiency in Microsoft Excel and data analysis. - Strong organizational skills and attention to detail. - Excellent communication and problem-solving abilities. - Experience in metal fabrication, welding, powder coating, machining, or assembly manufacturing environments. - Familiarity with CAD drawings and engineering documentation. - Experience with manufacturing ERP systems such as Fulcrum, JobBOSS, Epicor, NetSuite, SAP, or similar. - Lean Manufacturing or Continuous Improvement experience. Requirements - BOM accuracy. - Routing accuracy. - Engineering change implementation time. - Production data accuracy. - ERP transaction compliance. - Work order accuracy. - Reduction in production-related ERP errors. - Manufacturing process improvement initiatives completed. Reporting Structure - Reports to: Operations Manager / Director of Operations. - Works Closely With: Engineering, Production Supervisors, Production Planning, Purchasing, Quality, Operations Leadership. True Up is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.

• Demonstration of GE Healthcare ultrasound products at customer sites/hospitals and at conferences/exhibits/trade shows. • Assisting Sales Specialists by providing specialist sales support to ensure that all equipment is demonstrated to best advantage. • Post sales customer support product training both at customer sites/hospitals and on customer and/or GE lead education days/courses. • Maintaining contact with existing users ensuring ongoing customer satisfaction and confidence in using GE Healthcare ultrasound products • Always promote: Sell applications related products, while retaining good customer relationships (Software, Tip offerings) • Collect, analyse and communicate appropriate customer training and competitive information. • Maintain an effective Quality System and comply with the requirements of ISO0991, the Quality Policy and documented processes. • Comply with the EHS Policies and applicable laws and regulations. • Complete all mandatory EHS training. • Actively participate in accident & incident investigation and follow up. • Maintain defined levels of housekeeping & ensure a clean, clear workplace and participate in EHS inspections. • Identify and correct hazards and unsafe working conditions. • Supporting and assisting the Clinical Lead and Manager in the planning and implementation of service development, and other duties when requested.

Role Description The Specialist, Commercial Quality & Regulatory Affairs will prepare regulatory submissions and interact with regulatory agencies/health authorities to obtain and maintain product approvals. This individual will represent RA on project core teams, coordinate and prepare document packages for regulatory submissions from all areas of the company as well as for internal audits and inspections. Compile all materials required in submissions, license renewal, and annual registrations. Recommend changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. Keep abreast of changes of new or updated regulatory policies and issued guidance. This position reports to the Senior Manager, Commercial Quality & Regulatory Affairs and is part of the Center of Excellence located in Singapore and will be fully remote. In this role, you will have the opportunity to: - Lead pre-market and post-market regulatory activities for IVD devices, including preparation and submission of technical documentation, regulatory applications, change notifications, renewals, and responses to regulatory bodies and partners. - Maintain and manage regulatory intelligence and compliance at local, regional, and global levels, ensuring adherence to applicable regulations throughout the product lifecycle. - Oversee quality management processes and continuous improvement, including compliance operations, audits, CAPA, distributor and warehouse oversight, and acting as Quality Management Representative (QMR) when required. Qualifications - Bachelor’s degree with 6+ years of relevant experience or a certificate in medical devices with 3 years of experience or 4+ years of experience in the medical devices or a related industry. - Understands Regulatory Affairs concepts and is familiar with regulations/guidelines governing the development of diagnostic products. - Ability to prioritize, multitask, and organize work, succeed in a fast-paced environment with capability to be flexible and adaptable to meet business needs. Requirements - Ability to travel – 10%. Benefits - Comprehensive, competitive benefit programs that add value to our lives, including health care programs and paid time off.

Role Description The Specialist, Commercial Quality & Regulatory Affairs will prepare regulatory submissions and interact with regulatory agencies/health authorities to obtain and maintain product approvals. This individual will represent RA on project core teams, coordinate and prepare document packages for regulatory submissions from all areas of the company as well as for internal audits and inspections. - Compile all materials required in submissions, license renewal, and annual registrations. - Recommend changes for labeling, manufacturing, marketing, and clinical protocol for regulatory compliance. - Keep abreast of changes of new or updated regulatory policies and issued guidance. This position reports to the Senior Manager, Commercial Quality & Regulatory Affairs and is part of the Center of Excellence located in Singapore and will be fully remote. In this role, you will have the opportunity to: - Lead pre-market and post-market regulatory activities for IVD devices, including preparation and submission of technical documentation, regulatory applications, change notifications, renewals, and responses to regulatory bodies and partners. - Maintain and manage regulatory intelligence and compliance at local, regional, and global levels, ensuring adherence to applicable regulations throughout the product lifecycle. - Oversee quality management processes and continuous improvement, including compliance operations, audits, CAPA, distributor and warehouse oversight, and acting as Quality Management Representative (QMR) when required. Qualifications - Bachelor’s degree with 6+ years of relevant experience or a certificate in medical devices with 3 years of experience or 4+ years of experience in the medical devices or a related industry. - Understands Regulatory Affairs concepts and is familiar with regulations/guidelines governing the development of diagnostic products. - Ability to prioritize, multitask, and organize work, succeed in a fast-paced environment with capability to be flexible and adaptable to meet business needs. Requirements - Ability to travel – 10%. Benefits - Comprehensive, competitive benefit programs that add value to our lives. - Health care program. - Paid time off.