Director, Manufacturing Engineering

Work Flexibility: Onsite Summary:

The Director, Manufacturing Engineering and Maintenance provides strategic and operational leadership for a large technical organization responsible for advancing manufacturing capability, asset reliability and operational performance across high-volume, highly automated regulated manufacturing operations. This role sets the engineering and maintenance strategy, directs capital portfolio execution, drives automation and reliability roadmaps, and partners cross-functionally to deliver sustained improvements in safety, quality, service, cost, compliance and productivity. As a senior site leader, the Director builds organizational capability, develops technical talent and enables long-term business growth through disciplined execution, sound technical judgment and enterprise-level collaboration.

Essential Duties and Responsibilities:

• Lead the Manufacturing Engineering and Maintenance organization (over 100 engineers, technicians and leaders) responsible for sustaining, improving and advancing high-volume, highly automated medical device assembly, packaging, pharmaceutical mixing and converting processes.
• Translate site and business objectives into engineering and maintenance strategies, long-term roadmaps, team priorities, measurable goals and individual performance objectives that improve safety, quality, service, cost, productivity and compliance.
• Lead prioritization, planning and execution of complex engineering projects, automation programs, equipment upgrades, capacity expansions, cost reduction initiatives and business growth projects, balancing long-term capability development with urgent operational support needs.
• Manage $55M+ capital portfolio planning and execution, including business case development, project justification, budget adherence, resource allocation, risk management, vendor engagement and cross-functional stakeholder alignment.
• Provide technical leadership and decision-making support for manufacturing equipment, automation, controls, process performance, manufacturability, equipment reliability, asset lifecycle management and continuous improvement initiatives.
• Develop and improve maintenance strategy, asset reliability practices, preventive and predictive maintenance approaches, spare parts strategies and equipment lifecycle plans that reduce manufacturing loss, improve uptime and strengthen production continuity.
• Partner with Operations, Maintenance, Quality, EHS, Supply Chain, Finance and other functions to identify and resolve manufacturing issues, mitigate technical and operational risk, improve operating performance and ensure engineering work complies with safety, GMP, quality, regulatory and company standards.
• Lead and coach teams through structured problem solving, root cause analysis and continuous improvement efforts that address systemic safety, quality, compliance, equipment reliability, productivity and business continuity issues.
• Provide oversight for process FMEAs, control plans, change requests, SOPs, work instructions, manufacturing documentation, nonconformances, corrective and preventive actions, audit observations and other quality system deliverables where engineering ownership or support is required.
• Provide direction and coaching for equipment, process and cleaning validation strategies, protocols, execution, documentation and issue resolution in a regulated manufacturing environment.
• Establish and sustain engineering, automation, maintenance and documentation standards, best practices and governance processes that improve execution consistency and enable knowledge sharing across teams and sites.
• Manage relationships and performance expectations with equipment suppliers, automation integrators, contractors and technical service providers supporting capital projects, operational support and specialized engineering work.
• Partner with Advanced Operations to support new product introductions, process transfers, and launch readiness.
• Own capacity expansion and manufacturing scale-up activities by ensuring engineering, maintenance, validation, documentation and production support requirements are effectively planned and executed.
• Plan organizational capacity, define capability needs, allocate internal and external engineering resources, and build, coach and develop a high-performing technical organization that supports current site needs, succession planning and future business growth.
• Communicate complex technical plans, project status, risks, tradeoffs and recommendations to site leadership, cross-functional partners and senior stakeholders while modeling accountability, collaboration, urgency, sound judgment, inclusive leadership and a relentless focus on quality, compliance and business results.

Required Qualifications:

This role is based at the Cary, IL site and requires a full-time on-site presence Monday through Friday. Bachelor's degree in Engineering or required; Mechanical, Electrical, Industrial, or Manufacturing Engineering preferred. 15+ years of engineering and manufacturing experience, including significant expertise in manufacturing engineering, automation, and process improvement. 10+ years of leadership experience within medical device, pharmaceutical, or other highly regulated manufacturing environments. Proven success leading manufacturing engineering organizations supporting high-volume, automated operations, including development of engineering talent across multiple levels. Extensive experience leading large-scale automation initiatives and capital investment portfolios, including business case development, resource prioritization, budget management, and project execution. Strong technical expertise in manufacturing technologies, automation, controls, and mechanical systems, with the ability to translate technical concepts into operational results. Demonstrated success deploying Lean, continuous improvement, and structured problem-solving methodologies to drive safety, quality, delivery, and cost improvements. Experience with equipment and process validation in regulated manufacturing environments, including development and execution of validation strategies. Deep working knowledge of quality systems and operational excellence tools, including PFMEA, control plans, CAPA, nonconformance management, change control, SOPs, work instructions, and GMP-compliant documentation. Proven ability to partner cross-functionally with Operations, Quality, and Maintenance teams to improve equipment reliability, productivity, quality, safety and overall manufacturing performance. Experience developing and executing engineering strategies aligned with business objectives, while balancing long-term initiatives with day-to-day operational support. Strong leadership, communication, and influencing skills, with demonstrated ability to build relationships, lead change, coach teams, and effectively communicate with stakeholders at all organizational levels. Demonstrated ability to make sound, timely decisions, manage competing priorities and drive results in a fast-paced environment. Strong organizational and project management skills with a track record of delivering complex initiatives on time and within budget.

Preferred Qualifications:

• Experience supporting automated assembly, packaging, converting, or pharmaceutical manufacturing processes.
• Experience managing annual departmental or site capital budgets exceeding $15 million.
• Proven leader of leaders with experience managing large technical organizations of 100+ engineers, technicians, and leaders.

United States of America Pay Ranges:

USN: $155,900 - $259,700 USD Annual US10: $171,500 - $285,700 USD Annual View the U.S. work location and transparency guide to find the pay range for your location. Travel Percentage: 10%

Stryker Corporation is an equal opportunity employer:

Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer – M/F/Veteran/Disability. Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor’s legal duty to furnish information.

Stryker Technology and Work Flexibility Information:

Stryker Corporation will offer remote work flexibility, but the Director role requires full-time onsite presence at a Stryker facility. Remote – role allows to work the majority to 100% of time from an alternate workplace. Field-based – you can expect to regularly work a majority to 100% of time at customer facilities and has a set territory or expectation to travel within a set boundary. Onsite – role is 100% located at a Stryker facility. Hybrid – you can expect to regularly work in both an alternate workplace and a Stryker facility. Roles that are partially remote or co-located would qualify as hybrid, and the expectation to be onsite would be defined and agreed upon by your manager or supervisor.

Future Notes:

Stryker is one of the world’s leading medical technology companies and, together with its customers, is driven to make healthcare better. We offer innovative products and services in Orthopaedics, Medical and Surgical, and Neurotechnology and Spine that help improve patient and hospital outcomes. We are proud to be named one of the World’s Best Workplaces! For more information, visit: