Quality Engineer

Job Description

Job Description

Description:

Sr. Programmer - Quality Engineer

Durham, CT

Full-time | Permanent

Salaried | On-site

*We are not currently working with third party agencies on this role.

About Us:

Hobson & Motzer is now part of Vantedge Medical! Vantedge Medical is the premier metals-based med-tech solutions partner from concept to full-scale manufacturing. We are at the forefront of precision engineering and innovation, specializing in the development and manufacturing of vital components for medical markets such as Robotic Assisted Surgery, Orthopedics, Surgical Instruments, Dental, and more. Our teams work in unison, collaborating and problem-solving to serve the manufacturing needs of the top Medical Original Equipment Manufacturers (OEMs) around the globe. Making a difference in the lives of patients and their families drives us to go above and beyond every day. With a steadfast commitment to advancing medical technology, we take immense pride in the work we do – and have a lot of fun doing it.

Hobson & Motzer is a vertically integrated manufacturer of precision metal components and assemblies serving the needs of the medical device market and other advanced industries. We operate two manufacturing plants with primary operations—and headquarters—centrally located in Durham, CT; our Advanced Manufacturing Center is just a few miles away in Wallingford, CT. Description. Join an organization that has a reputation for outstanding leadership, innovation, and expertise. Our employees use their creativity and talent to invent new solutions, meet new demands, and offer the most effective services and solutions in the industry.

About this Opportunity: The Sr. Programmer-Quality Engineer is an expert in measurement science, leading teams to calibrate equipment, developing measurement systems (CMM’s, Vision Systems, 3D Scanners), analyzing complex data (GD&T, SPC), troubleshoot issues, and ensuring products through the manufacturing process.

Key responsibilities include Measurements Systems, Calibration & Standards, Data Analysis, Process Improvement, Leadership and Training.

In addition, the position serves as the Engineering Change Coordinator, responsible for creating Engineering Change Requests (ECRs) when new measurement methods are proven valid. This includes generating MSA’s and Capability Studies. Close collaboration with Engineering, Design and Quality teams is essential to ensure all documentation for new jobs is accurate, complete, and compliant with customer and regulatory requirements.

Responsibilities:

• Support and prepare PPAP submissions (all levels) including control plans, PFMEA, MSA, capability studies, and dimensional results; ensure timely and complete customer approval.
• Participate in APQP activities for new product launches, collaborating with Engineering and Production to ensure quality is built into the process from the start.
• Apply structured problem-solving methodologies (8D, DMAIC, Fishbone, 5-Why) to investigate non-conformances and support corrective and preventive action (CAPA) processes.
• Develop, review, and maintain Control Plans, PFMEAs, Work Instructions, and Methods of Inspection (MOIs) to ensure process compliance.
• Conduct process capability studies (Cp, Cpk) and use statistical tools (SPC, Minitab) to analyze data and support continuous improvement initiatives.
• Manage non-conforming material (NCMRs), dispositions, and supplier corrective action requests (SCARs).
• Collaborate with Engineering and Production teams on process improvements to reduce scrap, rework, and quality escapes.
• Support First Article Inspection (FAI) activities and customer-specific quality requirements.
• Utilize CMM, vision systems, and other metrology equipment to validate dimensional compliance; CMM programming experience is a plus.
• Assist in analyzing customer complaints and field returns; participate in cross-functional teams to resolve issues and implement corrective actions.
• Data Analysis, analyze inspection data, perform MSA’s, utilize statistical tools to drive continuous improvement.
• Maintain quality management system documentation in compliance with applicable standards and customer requirements.
• Support and collaborate with quality technicians and operators on inspection techniques and quality system requirements.
• Perform all other duties as assigned.

• Bachelor’s degree in Mechanical Engineering, Manufacturing Engineering, or a related technical field preferred; equivalent experience considered.
• Minimum 3–5 years of quality engineering experience in a precision manufacturing environment.
• Demonstrated expertise in PPAP/APQP processes and deliverables (all PPAP levels).
• Strong knowledge of PFMEA, Control Plans, MSA, and SPC methodologies.
• Proficiency with GD&T interpretation and application per ASME Y14.5.
• Hands-on experience with structured problem-solving tools: 8D, DMAIC, Fishbone, 5-Why.
• Familiarity with quality management standards: ISO 13485, AS9100, IATF 16949, or similar.
• Experience with Minitab or equivalent statistical software is required.
• Ability to read and interpret technical drawings, blueprints, and engineering specifications.
• CMM operation and/or programming experience (Calypso or similar) is a strong plus but not required.
• Solid communication skills, both written and verbal, with the ability to present findings to cross-functional teams and customers.
• Ability to work independently, prioritize multiple projects, and meet deadlines in a fast-paced environment.
• Basic-to-advanced math skills (as for GD&T calculations.).
• Ability to work independently, meet deadlines, and support cross-functional teams.
• Six Sigma Green Belt certification preferred.