GTO LCM Principal Process Engineer, Amsterdam

Job Function: Supply Chain Engineering Job Sub Function: Process Engineering Job Category: Scientific/Technology All Job Posting Locations: Nijmegen, Netherlands Job Summary

The Principal Process Engineer is responsible for providing engineering and technical support for complex production and processing equipment. The role involves managing the technical qualification of external manufacturers and their processes, supervising or aiding in the resolution of complex technical issues, and leading related activities for designated commodities. The position provides technical leadership, project management, and mentoring to junior engineers and team members, and explores and implements technical innovation needed to develop processes for the manufacture of medical devices.Duties&Responsibilities

Act as the technical lead for multiple small to large scale, complex projects and coordinate internal and external resources to achieve project goals. Support external manufacturers through qualification of supplier products and processes, analyzing and resolving supplier technical issues, and providing coaching and leadership.Represent both the supplier’s quality system and the J&J franchise quality system, ensuring technical plans comply with both. Partner with the New Product Development (NPD) community to assess technology, provide technical support, and support new product development and other product lifecycle activities. Lead cross‑functional teams in critical, complex projects with major impact on sales and profitability, and participate in technology and development of partnerships.Communicate business‑related issues or opportunities to management and ensure subordinates follow company guidelines related to health, safety, and environmental practices. Ensure compliance with all federal, state, local, and company regulations, policies, and procedures, and demonstrate understanding of GMP fundamentals, data integrity, and documentation practices.Perform other duties as assigned. Required Experience and Education

Minimum of a bachelor’s degree in Engineering or Science related field (Masters preferred). 6–8 years of relevant professional experience, including at least 5 years in process engineering (product development, process development, scale‑ups, CIPs, complex issue resolution, CAPA management, change control management, and process qualification).Required Knowledge, Skills&Abilities

Medical device (or highly regulated) industry production experience. Experience with NPD (preferred). Leadership and project management skills with ability to oversee development of others and execute complex work. Excellent written and oral communication and strong technical writing skills. Ability to manage multiple projects simultaneously and adjust priorities based on business needs.Technical support to manufacturing business units for complex process issues. Successful completion of several technical and/or business challenges and ability to lead cross‑functional teams. Knowledge of regulated industry quality systems and change control procedures. Six Sigma or process excellence experience (preferred).Ability to manage costs and budgets and prioritize commitments. Required Skills

Agile Decision Making Business Savvy Coaching Corrective and Preventive Action (CAPA) Crisis Management Critical Thinking Disruptive Innovations Emerging Technologies Industrial Hygiene Lean Supply Chain Management Organizing Process Control Process Engineering Product Costing Program ManagementProject Schedule Science, Technology, Engineering, Mathematics (STEM) Technical Research Preferred Skills

Design Excellence Additional Six Sigma or quality‑process experience Benefits

Base salary range:€68,600 – €119,600 per year. Benefits include an annual bonus target based on performance, vacation days, at least 12 weeks of parental leave, bereavement, caregiver, volunteer leave, well‑being reimbursement, financial, physical, and mental health programs, service‑anniversary awards, andmultiple insurance plans.

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