Principal Application Engineer/CNC Programmer

Stone Alliance Group; Berlin (CT); On-site; USD 80,000 - 110,000; Full time

Job summary

An established industry player is seeking a Principal Application Engineer/CNC Programmer to lead key production initiatives in a state-of-the-art facility. This role emphasizes continuous improvement and collaboration across teams to optimize manufacturing processes for high-precision medical devices. The ideal candidate will bring extensive experience in CNC programming and project management within regulated industries. Join a forward-thinking company that values innovation, quality, and professional growth, and be part of a team dedicated to excellence in medical device manufacturing.

Benefits

401k

Health Insurance

Dental Insurance

Vision Insurance

Paid Time Off

Qualifications

• 7+ years in regulated industries like medical devices or aerospace.
• Strong project management and manufacturing analysis skills.

Responsibilities

• Manage production deliverables including planning and process validations.
• Program CNC equipment for high-value medical device projects.
• Collaborate with cross-functional teams for process qualifications.

Skills

CNC Programming

Manufacturing Planning

Process Validation

Project Management

GD&T Interpretation

Continuous Improvement

Education

Bachelor's in Mechanical Engineering

Advanced Degree in Engineering

Tools

SolidWorks

Microsoft Office

Adobe Products

Job description

Principal Application Engineer/CNC Programmer

Join to apply for the Principal Application Engineer/CNC Programmer role at Stone Alliance Group

Our client, a leader in manufacturing devices and components for major medical device companies, is seeking a Principal Application Engineer.

They offer competitive compensation, comprehensive benefits including 401k, health/dental, vision, and paid time off. The facility is modern, clean, and equipped with state-of-the-art technology, emphasizing continuous improvement. The company is FDA-registered as a Class 2 and Class 3 Medical Device Manufacturer and ISO 13485 certified.

SUMMARY OF POSITION:

Reporting to the Sr. Engineering Manager, this role involves managing key production deliverables such as manufacturing planning, capacity planning, COGS estimation, process validations, capital equipment procurement, and production line setup. The company specializes in high-precision metal machining, finishing, assembly, and anodizing for Medical Devices.

ESSENTIAL FUNCTIONS:

• Potential direct-reporting responsibilities for site engineering personnel, depending on organizational structure.
• Develop and execute installation, operational, and process qualifications for customer manufacturing processes in collaboration with cross-functional teams.
• Program various CNC equipment across multiple sites for high-value projects, including milling, turning, grinding, multi-spindle, multi-axis, and Swiss-style operations for medical devices.
• Analyze drawings and models to determine dimensions, cutting tools, machine speeds, and feed rates aligned with shop processes and customer specifications.
• Participate in process development and design for manufacturability (DFM) projects.
• Revise and update CNC programs to improve efficiency and meet delivery deadlines.
• Coordinate with Quality Engineering to develop process control plans, inspection plans, and fixturing requirements.
• Create first-piece and in-process inspection plans.
• Design fixtures for post-processing operations.
• Adapt machine or equipment design to facility conditions.
• Incorporate inspection and testing requirements into production plans.
• Inspect machinery and tools to verify performance and initiate corrective actions as needed.
• Develop manufacturing processes suitable for statistical process control.
• Provide guidance on design concepts and specifications to optimize equipment and manufacturing techniques.
• Identify and support business growth opportunities, presenting recommendations to management.
• Act as a lead technical problem solver within the area of specialization.
• Deliver presentations to communicate project status, resolve problems, or promote business products.

QUALIFICATIONS:

• Bachelor's degree in mechanical engineering, biomedical engineering, or related field; advanced degree preferred.
• At least 7 years of experience in a regulated industry, preferably medical device or aerospace manufacturing.
• Project management experience, including planning, development, and execution.
• Ability to interpret drawings and GD&T specifications.
• Knowledge of manufacturing analysis, quality, and compliance standards.
• Experience transferring multidisciplinary products from development to production.
• High attention to detail.
• Proficiency in SolidWorks, Microsoft Office, and Adobe products.
• Experience with continuous improvement initiatives, including Kaizen events and lean manufacturing principles.