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Manufacturing Systems Engineer - Job Opportunity at Terumo Aortic

Renfrew, United Kingdom
Full-time
Mid-level
Posted: June 3, 2025
On-site
£45,000 - £65,000 annually based on the mid-level experience requirements, specialized MES expertise, and Terumo Aortic's position as a premium medical device manufacturer. The salary range reflects the combination of manufacturing systems expertise, medical device industry premiums, and Scottish market conditions where specialized engineering talent commands competitive compensation.

Benefits

Comprehensive sick pay coverage providing financial security during health-related absences, exceeding statutory minimums
Free on-site parking eliminating daily commuting costs and providing convenience in urban locations
Company pension scheme with employer contributions securing long-term financial stability and retirement planning
Additional leave entitlement beyond statutory requirements supporting work-life balance and personal time
Cycle to work scheme offering tax-efficient bicycle purchases promoting health and sustainable commuting
Subsidized or complimentary food services reducing daily expenses and fostering workplace community
Guaranteed on-site parking spaces ensuring reliable daily access without urban parking challenges
Performance-based bonus scheme providing additional compensation tied to individual and company success

Key Responsibilities

Champion MES (Manufacturing Execution System) implementation across the organization while leading critical change management initiatives that drive operational transformation and employee adoption
Provide strategic MES consultancy and advisory services to all business units, positioning yourself as the internal expert driving manufacturing intelligence and operational efficiency
Maintain and optimize master data integrity for manufacturing systems, ensuring accurate information flow that supports critical business decisions and regulatory compliance
Lead comprehensive testing, maintenance, and enhancement of existing manufacturing systems, directly impacting production reliability and operational continuity
Drive new product introduction processes by ensuring manufacturing systems readiness, facilitating seamless product launches and time-to-market optimization
Conduct advanced data analysis and create executive-level reports that inform strategic manufacturing decisions and identify optimization opportunities
Foster cross-functional collaboration with engineering, operations, and internal stakeholders to align manufacturing systems with business objectives
Develop and implement corrective action plans addressing quality issues within manufacturing systems, directly impacting product quality and customer satisfaction
Support strategic plant initiatives and adapt to evolving responsibilities that align with organizational growth and personal career development

Requirements

Education

Degree in related subject

Experience

5+ years relevant previous experience in a high quality manufacturing environment

Required Skills

Proficient use of ERP or MES applications such as Opcenter, QAD, SAP Problem solving and analytical skills Good communication skills Ability to adapt to new skills (technical & quality) Demonstrate knowledge of product, process & people movement Process Engineering, Business and IT- Analytical skills required Strong teamworking skills A high level of attention to detail
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Sauge AI Market Intelligence

Industry Trends

Medical device manufacturing is experiencing unprecedented digital transformation driven by Industry 4.0 initiatives, with MES systems becoming critical for maintaining regulatory compliance while optimizing production efficiency. Companies are investing heavily in integrated manufacturing systems to meet stringent FDA and CE marking requirements while reducing time-to-market for life-saving devices. The global medical device market is projected to reach $671 billion by 2025, with manufacturing systems engineers playing pivotal roles in scaling production capabilities while maintaining the highest quality standards. This growth is particularly strong in cardiovascular devices, where Terumo Aortic operates, driven by aging populations and increasing prevalence of cardiovascular diseases. Regulatory environments are becoming increasingly complex with new EU MDR requirements and evolving FDA guidelines, making manufacturing systems expertise crucial for compliance management. Companies are seeking professionals who can bridge the gap between traditional manufacturing and modern digital quality systems to ensure seamless regulatory submissions and audits. Supply chain resilience has become a strategic priority following global disruptions, with manufacturing systems engineers leading initiatives to implement predictive analytics, real-time monitoring, and flexible production systems that can adapt to supply constraints while maintaining quality standards.

Role Significance

Typically works within a manufacturing engineering team of 8-12 professionals while collaborating across multiple departments including quality assurance, production operations, IT systems, and regulatory affairs. The role often involves leading project teams of 4-6 members for system implementations and improvement initiatives.
This role represents a senior individual contributor position with significant organizational influence, requiring the candidate to serve as the internal expert and change agent for manufacturing systems across the entire organization. The position carries substantial responsibility for system integrity and strategic initiatives while providing a platform for technical leadership and cross-functional collaboration.

Key Projects

Implementation of comprehensive MES upgrades across production lines to enhance real-time monitoring, batch tracking, and regulatory compliance reporting while minimizing production disruptions and ensuring seamless data integration with existing ERP systems Leading new product introduction projects that require manufacturing systems configuration, testing protocols development, and validation documentation to support regulatory submissions while ensuring scalable production capabilities Development of advanced analytics dashboards and reporting systems that provide manufacturing intelligence to executive leadership, enabling data-driven decisions for capacity planning, quality improvements, and operational efficiency optimization

Success Factors

Deep technical expertise in MES and ERP systems combined with practical understanding of medical device manufacturing processes, enabling effective system optimization while maintaining regulatory compliance and quality standards throughout all implementations and modifications Strong change management and communication skills to successfully lead organizational transformation initiatives, particularly the ability to translate complex technical concepts into business benefits while managing resistance and ensuring user adoption across diverse stakeholder groups Analytical mindset with proven ability to identify root causes of manufacturing issues and develop systematic solutions that address both immediate problems and underlying systemic challenges, demonstrated through successful quality improvement initiatives and system optimizations Cross-functional collaboration capabilities that enable effective partnership with engineering, operations, quality, and IT teams while maintaining focus on business objectives and managing competing priorities in a fast-paced manufacturing environment

Market Demand

High demand driven by the critical shortage of manufacturing systems professionals with medical device experience, particularly those with MES expertise in regulated environments. The combination of technical systems knowledge and quality manufacturing experience creates a valuable skill set that is increasingly sought after as medical device companies modernize their production capabilities.

Important Skills

Critical Skills

MES and ERP systems proficiency is absolutely essential as these platforms form the backbone of modern medical device manufacturing, with systems like Opcenter, QAD, and SAP requiring specialized knowledge to configure, maintain, and optimize for regulatory compliance while supporting complex production workflows and quality tracking requirements Analytical and problem-solving capabilities are fundamental to success in this role, as manufacturing systems engineers must diagnose complex technical issues, analyze production data to identify improvement opportunities, and develop systematic solutions that address both immediate operational needs and long-term strategic objectives Communication and collaboration skills are critical for driving organizational change and managing cross-functional relationships, particularly important when implementing new systems or processes that affect multiple departments and require buy-in from diverse stakeholder groups with varying technical backgrounds

Beneficial Skills

Project management certification and experience would enhance effectiveness in leading system implementations and improvement initiatives across complex organizational structures Knowledge of regulatory requirements specific to medical devices (FDA, CE marking, ISO 13485) would provide additional value in ensuring manufacturing systems support compliance objectives Data analytics and visualization skills using tools like Power BI, Tableau, or similar platforms would enable more sophisticated reporting and insights generation from manufacturing data Understanding of Lean Manufacturing and Six Sigma methodologies would complement systems engineering expertise by providing structured approaches to process improvement and waste elimination

Unique Aspects

This role offers direct impact on life-saving medical device production, where manufacturing systems improvements translate directly into better patient outcomes and enhanced surgical capabilities for cardiovascular procedures worldwide
Opportunity to work with cutting-edge MES technology in a highly regulated environment, providing experience with both advanced manufacturing systems and complex regulatory compliance requirements that are highly transferable across the medical device industry
Access to Terumo Corporation's global network and resources while working in a specialized cardiovascular focus area, offering both international career opportunities and deep expertise development in a critical medical field
Combination of technical systems engineering with change management responsibilities, providing a unique skill development opportunity that bridges engineering expertise with organizational leadership capabilities

Career Growth

Progression to senior individual contributor roles typically occurs within 2-3 years with demonstrated system implementation success, while management positions generally become available within 4-6 years with proven leadership capabilities and strategic project delivery.

Potential Next Roles

Senior Manufacturing Systems Engineer with expanded responsibilities for multiple product lines and strategic system architecture decisions Manufacturing Engineering Manager overseeing teams of systems engineers and manufacturing specialists Plant Engineering Manager with broader operational responsibilities including maintenance, facilities, and continuous improvement initiatives Digital Manufacturing Lead focusing on Industry 4.0 implementations and advanced manufacturing technologies

Company Overview

Terumo Aortic

Terumo Aortic is a specialized division of Terumo Corporation, a global leader in medical technology with over 100 years of innovation in healthcare solutions. The company focuses specifically on aortic and cardiovascular surgical products, developing life-saving medical devices including heart valves, vascular grafts, and surgical instruments used in complex cardiac procedures worldwide.

Terumo Aortic holds a strong position in the global cardiovascular medical device market, competing with industry leaders like Medtronic, Abbott, and Edwards Lifesciences. The company leverages Terumo Corporation's extensive resources and global reach while maintaining specialized focus on cardiovascular solutions, allowing for both innovation investment and market responsiveness.
The Renfrew facility serves as a key European manufacturing and development center, supporting Terumo Aortic's global operations while providing access to the UK's strong life sciences ecosystem. This location offers exposure to international markets while benefiting from the UK's regulatory expertise and proximity to major European healthcare markets.
Terumo Aortic emphasizes a patient-focused culture where every role contributes directly to life-saving medical solutions, creating a meaningful work environment with strong emphasis on quality, safety, and continuous improvement. The company culture combines Japanese corporate values of respect and continuous improvement with dynamic Western innovation approaches, fostering both stability and growth opportunities.
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