Earnbetter

Job Search Assistant

Senior Process Development Engineer - Medical Device Industry

Gilero • Pittsboro, NC 27312 • Posted 4 days ago via LinkedIn

Boost your interview chances in seconds

Tailored resume, cover letter, and cheat sheet

In-person • Full-time • Senior Level

Job Highlights

Using AI ⚡ to summarize the original job post

The Senior Process Development Engineer at Gilero is responsible for developing new manufacturing systems for emerging technologies to support the production of medical devices under device regulations and standards. This role involves designing and implementing manufacturing processes, leading projects from developmental pilots to full commercial production, and working with automated equipment and processes for complex device assembly and testing.

Responsibilities

  • Specify and manage external build contractors, install, troubleshoot, and validate automated equipment and processes for complex device assembly and testing.
  • Develop and deliver new manufacturing process capabilities as needed including process selection, characterization and qualification utilizing designed experiment methodology (DOE).
  • Evaluate new device designs for manufacturability (DFM/DFA).
  • Establish process flow and line layouts to achieve efficient, flexible, and scalable manufacturing cells.
  • Utilizes Lean Thinking, Six Sigma and 5S concepts when creating new or improving existing processes.
  • Specify new process equipment for manual and fully-automated production lines.
  • Write and execute protocols to assess manufacturing process capability (IQ/OQ/PQ).
  • Generate CAD models for test or assembly fixtures.
  • Establish maintenance requirements for new equipment.
  • Evaluate the impact of new processes introductions on critical environments.
  • Assess and implement process changes as required by customer request, in response to manufacturing quality issues, or design changes.
  • Perform process risk analysis through PFMEA activities to support new or existing processes.
  • Maintain Device Master Record (DMR) and ensure documents are complete, accurate, and current.
  • Participate in manufacturing investigations/CAPA resolutions to identify improvements to the manufacturing processes.
  • Support quality audits of manufacturing processes.
  • Drive Continuous Improvement activities within the manufacturing area.
  • Develop processes and rates for customer quotations.
  • Facilitate design transfer of existing products to and from other manufacturing sites.
  • Lead project activities through the management of budgets, resources, timelines, and deliverables.

Qualifications

Required

  • BS in Engineering or equivalent technical degree.
  • Minimum 5 years relevant experience in manufacturing medical devices.
  • Knowledge of medical device regulations (FDA/ISO).
  • Proven ability to lead a manufacturing program.
  • Experience incorporating vision systems into manufacturing equipment for in-process inspection and/or motion control.
  • Skills and experience with Electromechanical/Automation.
  • Experience with SolidWorks, Pro/Engineer and/or other 3D CAD modeling software.

Preferred

  • Experience with drug filling and handling for combination products.
  • Ability to program PLC, Arduino, or other motion controllers.
  • Excellent communication skills (oral and written).
  • Proficient computer skills, including Excel and Word.

Full Job Description

Gilero is growing and looking for an experienced Senior Process Engineer to support development and manufacturing of exciting assembly automation projects for medical and pharmaceutical delivery devices. The position is located at our Pittsboro, NC manufacturing plant.


Job Summary:

The position is responsible for developing new manufacturing systems for emerging technologies to support the production of medical devices under device regulations and standards (ISO 13485 and FDA 21 CFR Part 820). In this role, you will be responsible for designing and implementing manufacturing processes and leading projects on a scale that can range from developmental pilots to full commercial production.


Duties:

  • Specify and manage external build contractors, install, troubleshoot, and validate automated equipment and processes for complex device assembly and testing.
  • Develop and deliver new manufacturing process capabilities as needed including process selection, characterization and qualification utilizing designed experiment methodology (DOE)
  • Evaluate new device designs for manufacturability (DFM/DFA)
  • Establish process flow and line layouts to achieve efficient, flexible, and scalable manufacturing cells
  • Utilizes Lean Thinking, Six Sigma and 5S concepts when creating new or improving existing processes.
  • Specify new process equipment for manual and fully-automated production lines
  • Write and execute protocols to assess manufacturing process capability (IQ/OQ/PQ)
  • Generate CAD models for test or assembly fixtures
  • Establish maintenance requirements for new equipment
  • Evaluate the impact of new processes introductions on critical environments
  • Assess and implement process changes as required by customer request, in response to manufacturing quality issues, or design changes.
  • Perform process risk analysis through PFMEA activities to support new or existing processes.
  • Maintain Device Master Record (DMR) and ensure documents are complete, accurate, and current including process routers, inspection plans, temporary deviations, and non-conformances.
  • Participate in manufacturing investigations/CAPA resolutions to identify improvements to the manufacturing processes.
  • Support quality audits of manufacturing processes
  • Drive Continuous Improvement activities within the manufacturing area to meet and exceed operational objectives and goals
  • Develop processes and rates for customer quotations in response to inquiries while working with Tooling, Engineering, Purchasing, and Customer Service to obtain needed information
  • Facilitate design transfer of existing products to and from other manufacturing sites.
  • Lead project activities through the management of budgets, resources, timelines, and deliverables
  • Provide engineering expertise in resolving specific technology issues during development and provide support to the production team during ramp and sustaining activities
  • Provide engineering expertise to the sales and customer service teams in working with customers including delivering technical presentations
  • Communicate effectively with customers and vendors in a technical capacity
  • May serve as an electromechanical/automation SME within the department, helping to build this skillset within the team.


Skills/Qualifications:

  • BS in Engineering or equivalent technical degree.
  • Minimum 5 years relevant experience in manufacturing medical devices.
  • Knowledge of medical device regulations (FDA/ISO)
  • Proven ability to lead a manufacturing program
  • Experience incorporating vision systems into manufacturing equipment for use in in-process inspection and/or motion control.
  • Skills and experience with Electromechanical/Automation a strong plus.
  • Experience with drug filling and handling for combination products, strong plus.
  • Ability to program PLC, Arduino, or other motion controllers, strong plus.
  • Experience with SolidWorks, Pro/Engineer and/or other 3D CAD modeling software, preferred.


Personal Attributes:

  • Meets Gilero Core Values: Collaboration, Integrity, Innovation and Excellence
  • Comfortable and productive in a fast-paced, entrepreneurial environment
  • A self-starter seeking a career opportunity with potential for internal advancement, seeking responsibility for core activities and providing high quality service to internal and to external clients
  • Commitment to excellence and quality service to external and internal customer
  • Commitment to established policies and procedures, while contributing to continuous improvements
  • Excellent communication skills (oral and written)
  • Proficient (or better) computer skills, including Excel and Word


About Pittsboro and facility location:

  • Gilero’s facility is located in downtown Pittsboro within walking distance to multiple restaurants, breweries, boutique shops, and entertainment.
  • 30 miles from RTP
  • 8 miles from Jordan Lake recreation area
  • 15 miles from Chapel Hill
  • 35 miles from Raleigh
  • 2.5 hr drive to NC beaches
  • 2.5 hr drive to NC mountains
  • Multiple contemporary neighborhoods are under construction including Chatham Park and Asteria (a Disney community).
  • Located in Chatham County, the area is poised to grow substantially with multiple new industries including semi-conductor, electric vehicles, and battery manufacturing.