Manufacturing Engineer (Class II and III Interventional Devices)

Aptyx; Charlotte (NC); On-site; USD 60,000 - 95,000; Full time

Job summary

Aptyx is seeking a Manufacturing Engineer I–II to support and advance the manufacture of interventional medical devices in a regulated environment. You will work closely with R&D, Operations, Quality, Supply Chain, and customers to transfer products from development into scalable production.

Level I focuses on foundational capabilities while Level II owns processes, leads projects, and resolves complex issues, driving transfer and continuous improvement across manufacturing functions.

Qualifications

• Experience in medical device manufacturing.
• Ability to work hands-on in a production environment.
• Understanding of IQ/OQ/PQ and process validation.
• Experience with product or process transfer from development to production.
• Strong written and verbal communication and cross-functional collaboration.

Responsibilities

• Provide hands-on engineering support within the manufacturing environment to ensure quality, delivery, productivity, and cost.
• Develop, implement, and improve manufacturing processes for interventional medical devices, including catheters and implants.
• Support daily production by troubleshooting equipment, tooling, materials, processes, and product-related issues.
• Lead or participate in transfer planning, production launches, and ramp-up activities.
• Conduct process validation, CAPA, and continuous improvement activities.

Skills

Hands-on engineering

Problem solving

Lean Six Sigma

Cross-functional collaboration

Manufacturing processes

Education

Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or related

Tools

SolidWorks

ERP systems

Job description

Manufacturing Engineer I–II – Interventional Medical DevicesPosition Summary The Manufacturing Engineer I–II is responsible for supporting and advancing the manufacturing of Class II and Class III interventional medical devices, including catheters, implants, and other complex disposable medical devices. This position works directly within the production environment to develop, transfer, validate, launch, troubleshoot, and continuously improve manufacturing processes. The Manufacturing Engineer partners closely with R&D, Operations, Quality, Supply Chain, and customers to transfer products and processes from development into repeatable, scalable production. The role requires a hands‑on engineering approach, with a strong understanding of manufacturing processes, equipment, tooling, process validation, and production requirements within a regulated medical device environment. At Level I, the engineer develops foundational manufacturing engineering capabilities while supporting production transfers, process development, validation, and continuous improvement activities. At Level II, the engineer independently owns manufacturing processes and transfer activities, leads technical projects, resolves complex production issues, and serves as a key engineering partner to Operations and R&D.

Manufacturing Engineering & Production Support

• Provide hands‑on engineering support within the manufacturing environment to ensure processes consistently meet requirements for quality, delivery, productivity, and cost.
• Develop, implement, and improve manufacturing processes for interventional medical devices, including catheters, implants, and other complex disposable products.
• Support daily production by troubleshooting equipment, tooling, materials, processes, and product‑related issues.
• Investigate manufacturing issues using structured problem‑solving and root‑cause analysis techniques.
• Develop and implement corrective and preventive actions that improve process capability, yield, reliability, and throughput.
• Partner with Operations to establish efficient and repeatable manufacturing methods.
• Support production builds, pilot runs, first builds, process trials, and production ramp‑up activities.
• Develop operator training and manufacturing process documentation as required.

Product & Process Transfer

• Support the transfer of new and existing medical device products from R&D and development into production.
• Translate product designs and development requirements into practical, manufacturable production processes.
• Develop manufacturing processes, equipment, tooling, fixtures, workstations, and production methods required to support product launch.
• Participate in transfer planning, including identification of manufacturing requirements, equipment, tooling, materials, labor, capacity, and process risks.
• Execute manufacturing activities associated with product transfers, engineering changes, process changes, and production launches.
• Work closely with R&D Engineering to ensure designs are transferred into production with appropriate consideration for manufacturability, process capability, quality, and cost.
• Identify and resolve transfer issues prior to and during production launch.
• Support successful transition from development builds to stable, repeatable production.

Process Development & Equipment Implementation

• Develop and optimize manufacturing processes for complex interventional medical devices.
• Evaluate, select, and implement manufacturing equipment, tooling, fixtures, and technologies.
• Support equipment procurement, installation, commissioning, and qualification.
• Develop process parameters and operating windows that support consistent product quality and manufacturing performance.
• Conduct process trials and engineering experiments to evaluate and improve manufacturing methods.
• Perform capacity analysis, line balancing, time studies, and process‑flow analysis.
• Evaluate opportunities for automation and semi‑automation to improve quality, productivity, and scalability.
• Work with equipment and tooling suppliers to resolve technical issues and implement manufacturing solutions.

Process Validation & Risk Management

• Develop and execute process validation activities in accordance with the Aptyx Quality System and applicable medical device requirements.
• Prepare and execute IQ, OQ, PQ, TMV, Gage R&R, MSA, and other applicable validation activities.
• Develop and maintain manufacturing process documentation and validation records.
• Support development and maintenance of pFMEAs, control plans, Master Validation Plans, process specifications, and related risk‑management documentation.
• Identify manufacturing risks and establish appropriate process controls.
• Ensure validation activities demonstrate that manufacturing processes are capable of consistently producing product that meets established requirements.
• Maintain accurate, complete, and audit‑ready engineering and validation documentation.

Production Launch & Ramp‑Up

• Support manufacturing readiness activities from development through production launch.
• Develop manufacturing processes and documentation necessary to support new product introduction.
• Coordinate engineering activities required for pilot builds, first production runs, and production ramp‑up.
• Monitor early production performance and identify opportunities for process stabilization.
• Partner with Operations and Quality to establish appropriate process controls and production metrics.
• Evaluate production capacity and resource requirements to support current and future demand.
• Support transition of processes from initial launch to sustained production ownership.

Continuous Improvement & Lean Manufacturing

• Identify and implement opportunities to improve safety, quality, delivery, productivity, yield, and cost.
• Apply Lean Manufacturing and Six Sigma principles to improve manufacturing processes.
• Analyze scrap, rework, downtime, cycle time, labor utilization, and other manufacturing performance indicators.
• Lead or participate in continuous improvement projects that produce measurable operational results.
• Conduct time studies and develop standard work to improve process consistency and efficiency.
• Identify opportunities to reduce waste, improve flow, increase capacity, and optimize labor utilization.
• Evaluate manufacturing costs and identify opportunities to reduce COGS without compromising quality or regulatory requirements.

Design for Manufacturability

• Partner with R&D Engineering during product development to ensure designs can be efficiently and consistently manufactured.
• Participate in DFM reviews and provide manufacturing input on product design, materials, tolerances, assembly methods, and process requirements.
• Recommend design changes that improve manufacturability, yield, reliability, quality, and cost.
• Identify potential manufacturing challenges early in the development process and work collaboratively with R&D to resolve them.

Quality System & Compliance

• Follow the Aptyx Quality System, applicable SOPs, work instructions, and requirements identified within the Training Matrix.
• Ensure manufacturing engineering activities comply with applicable medical device regulations and internal procedures.
• Support compliance with requirements applicable to Class II and Class III medical devices.
• Maintain appropriate engineering records and documentation to support internal and external audits.
• Participate in investigations, CAPA, nonconformance, change control, and other quality‑system activities as required.

Engineering Change & Documentation

• Create, review, and maintain manufacturing engineering documentation, including:
  • Work instructions
  • Process specifications
  • Manufacturing procedures
  • Bills of material (BOMs)
  • Routings
  • Process flow diagrams
  • Control plans
  • Validation protocols and reports
  • Engineering change documentation
• Maintain accurate manufacturing and engineering information within ERP and other applicable systems.
• Ensure manufacturing documentation accurately reflects current production processes.

Supplier & Material Support

• Work with suppliers on materials, tooling, equipment, and manufacturing processes.
• Support supplier qualification and validation activities.
• Investigate material‑or supplier‑related manufacturing issues.
• Support material changes and process changes through appropriate engineering and quality‑system processes.
• Partner with Supply Chain and Quality to resolve technical and material issues affecting production.

Cross‑Functional & Customer Collaboration

• Collaborate with R&D, Operations, Quality, Supply Chain, and other functional teams to resolve manufacturing and transfer issues.
• Communicate technical information, project status, risks, and manufacturing requirements clearly to internal stakeholders.
• Participate in customer meetings and technical discussions related to manufacturing transfer, process development, validation, and production readiness.
• Build effective working relationships across functions to ensure successful product transfer and production execution.
• Escalate technical, quality, schedule, or resource risks appropriately.

Project Execution

• Support or lead manufacturing engineering projects associated with new product introduction, product transfer, process improvement, equipment implementation, and production expansion.
• Develop project plans, identify required resources, track deliverables, and communicate project status.
• At Level II, independently manage assigned engineering projects with responsibility for scope, timing, technical execution, and deliverables.
• Ensure engineering activities remain aligned with customer requirements, quality expectations, manufacturing needs, and business objectives.

Qualifications

• Experience in medical device manufacturing, manufacturing engineering, process engineering, or product transfer required.
• Experience supporting the manufacturing of interventional medical devices, catheters, implants, or other complex disposable medical devices strongly preferred.
• Working knowledge of manufacturing processes, equipment, tooling, materials, and process development.
• Demonstrated ability to work hands‑on in a production environment.
• Understanding of medical device manufacturing requirements and process validation.
• Experience with product or process transfer from development into production preferred.
• Experience with Lean Manufacturing, Six Sigma, and structured problem‑solving preferred.
• Experience with SolidWorks or comparable CAD software preferred.

Education

• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, Manufacturing Engineering, or a related engineering discipline required.

Experience

Manufacturing Engineer I

• 1+ years of relevant engineering or manufacturing experience.
• Medical device manufacturing experience preferred.
• Demonstrated understanding of fundamental engineering and manufacturing principles.

Manufacturing Engineer II

• 2–5 years of engineering experience, preferably within medical device manufacturing.
• Demonstrated experience with manufacturing process development, product/process transfer, validation, and production support.
• Experience independently troubleshooting and improving manufacturing processes.
• Experience leading engineering projects preferred.

Skills, Knowledge & Abilities

• Strong understanding of manufacturing processes and production equipment.
• Knowledge of process development and transfer methodologies.
• Understanding of IQ, OQ, PQ, TMV, Gage R&R, and MSA.
• Ability to interpret engineering drawings, specifications, and product requirements.
• Proficiency with Microsoft Office and engineering documentation systems.
• Experience with CAD software such as SolidWorks preferred.
• Working knowledge of ERP systems.
• Strong analytical, troubleshooting, and problem‑solving skills.
• Ability to work effectively in a hands‑on production environment.
• Strong written and verbal communication skills.
• Ability to manage multiple priorities and work effectively in a fast‑paced environment.
• Ability to collaborate effectively with technical and non-technical teams.
• Ability to recognize process risks and make sound engineering recommendations.

Core Competencies

• Manufacturing & Technical Excellence

Level I

Applies foundational engineering principles and develops manufacturing knowledge with guidance.

Level II

Independently develops, improves, and troubleshoots manufacturing processes and equipment.

• Product & Process Transfer

Level I

Supports product and process transfers and executes assigned transfer activities.

Level II

Independently owns manufacturing transfer activities and ensures successful transition into production.

• Quality & Validation

Level I

Supports validation activities and maintains accurate engineering documentation.

Level II

Independently develops and executes validation activities and ensures processes are robust and compliant.

• Production Problem Solving

Level I

Uses structured problem‑solving techniques to identify and address manufacturing issues.

Level II

Leads complex root‑cause investigations and implements sustainable corrective actions.

• Continuous Improvement

Level I

Identifies opportunities for improvement and participates in Lean and continuous improvement activities.

Level II

Leads improvement initiatives and delivers measurable improvements in quality, productivity, capacity, and cost.

• Project Ownership

Level I

Completes assigned engineering activities and meets established project commitments.

Level II

Owns engineering projects, deliverables, timelines, and technical execution with minimal oversight.

• Cross‑Functional Collaboration

Level I

Effectively communicates with team members and escalates issues when appropriate.

Level II

Serves as a technical partner to Operations, R&D, Quality, Supply Chain, and customers and drives cross‑functional alignment.

• Business & Cost Awareness

Level I

Understands basic manufacturing cost drivers and identifies opportunities for improvement.

Level II

Evaluates manufacturing costs, capacity, labor, yield, and process performance to support cost‑reduction and operational decisions.

Measurement of Performance

• Successful transfer and launch of products and processes into production.
• Manufacturing processes that consistently meet quality, delivery, productivity, and cost requirements.
• Timely and accurate completion of validation and engineering documentation.
• Effective resolution of production and process issues.
• Improvements in yield, throughput, capacity, cycle time, scrap, and cost.
• Successful implementation of equipment, tooling, and manufacturing processes.
• Effective collaboration with Operations, R&D, Quality, Supply Chain, and customers.
• Successful execution of assigned engineering projects.
• Demonstrated growth in technical capability, independence, and ownership.

Physical Demands of Position

The physical demands described are representative of those required to successfully perform the essential functions of this position. Reasonable accommodations may be made. This position requires regular sitting, standing, walking, and use of hands for computer, laboratory, equipment, and manufacturing activities. The employee may be required to work directly on or around manufacturing equipment and production processes. The role operates in both laboratory and manufacturing environments with variable conditions. Effective verbal and written communication and standard vision and hearing capabilities are required.

Salary: $60000 - $95000 per year