Jobs at Resonetics

Leads and mentors manufacturing engineering teams supporting high-volume contract manufacturing and medical device production. Responsibilities include process and equipment development, product launches, validation, quality investigations, capital planning, safety compliance, tooling support, continuous improvement, technical documentation, customer interactions, and production cost quoting. Requires extensive supervisory and high-tech manufacturing experience, ISO expertise, and knowledge of machining, tooling, engineering standards, and analytical methods.

Manages complex production and material planning, balancing demand, capacity, inventory, materials, and delivery commitments. Leads cross-functional planning, ERP data and parameter management, inventory and purchasing analysis, KPI monitoring, recovery planning, new product transitions, and continuous improvement initiatives. Serves as the site planning and ERP subject matter expert while identifying risks and driving corrective actions in a regulated manufacturing environment.

Leads plastic injection molding process transitions, validations, improvements, and optimization through manufacturing control. Manages scientific molding validations, troubleshooting, corrective actions, documentation, customer project meetings, and cross-functional manufacturing support. Requires engineering expertise, hands-on machine operation, statistical validation analysis, Lean Six Sigma, project management, budgeting, and knowledge of mold tooling and automation. Ensures compliance with quality, safety, and regulatory requirements while supporting multiple initiatives and meeting project deadlines.

Leads end-to-end development of complex interventional medical devices, including concept generation, SolidWorks design, prototyping, testing, verification, risk management, and design controls. Serves as technical and project lead for customer programs, manages schedules and decisions, supports quality compliance and clinical studies, mentors junior engineers, and drives process improvement across multiple concurrent projects.

Leads the development, optimization, validation, and implementation of medical device manufacturing processes. Responsibilities include coordinating projects, equipment and facility planning, manufacturing launches, process and quality analysis, engineering change orders, production transfers, capital expenditure justification, automation initiatives, and lean manufacturing improvements. Provides technical leadership and coaching while collaborating cross-functionally with operations, quality, regulatory, finance, and clinical teams.

Leads complex medical device product development programs from concept through commercialization. Manages cross-functional teams, project scope, schedules, budgets, risks, quality, vendors, resources, and customer deliverables. Establishes project management practices, reports milestones and performance, resolves quality issues, and ensures compliance with regulated-industry requirements. Coaches team members and coordinates with finance, accounting, human resources, procurement, manufacturing, and quality functions.

Oversee lab operations and engineering teams responsible for medical device prototyping and micro-manufacturing projects. Manage resource allocation, project delivery, quality, throughput, customer communications, and cross-functional collaboration. Mentor engineering leaders, resolve technical and operational challenges, monitor site metrics, drive continuous improvement, and ensure compliance with quality standards and medical device manufacturing requirements.

The NPI Engineer develops and transfers medical device manufacturing processes from design through commercial launch. Responsibilities include designing tooling and fixtures, supporting production lines, improving processes, troubleshooting equipment, preparing documentation, conducting process and equipment validations, performing risk assessments, analyzing data, and training production personnel. The role requires collaboration with product development, quality, supply chain, and production teams in a regulated manufacturing environment.

Leads and develops a manufacturing engineering team responsible for improving existing production processes and transitioning new products into production. Drives continuous improvement in yield, throughput, labor efficiency, quality, and cycle time; oversees process documentation and validation activities including OQ and PQ. Collaborates with production, value streams, new product development, and sales on process design, costing, and compliance in FDA- and ISO-regulated environments.

Designs, develops, integrates, commissions, and supports automated machinery and manufacturing systems. Develops controls software for PLCs, HMIs, motion, vision, robotics, safety, and industrial networks. Leads system architecture, troubleshooting, customer-site startups, documentation, acceptance testing, and production launches. Manages controls deliverables across projects, collaborates with customers and cross-functional teams, mentors junior engineers, and drives controls standardization. Requires domestic and international travel of approximately 10% to 25%.

Manages manufacturing engineering and NPI activities, engineering staff, departmental priorities, processes, and procedures. Resolves complex technical and operational issues, drives process improvements, applies lean and Six Sigma principles, mentors employees, and collaborates across departments. The role supports medical device manufacturing, capacity and facility optimization, process development and validation, quality standards, and continuous improvement initiatives.

Supports NPI and process transfer of Nitinol-based medical device manufacturing technologies into production. Responsibilities include process validation, documentation, cost and cycle-time baselining, root-cause analysis, statistical process characterization, yield improvement, equipment qualification, troubleshooting, operator training, and cross-functional project leadership. The role collaborates with Process Development, Quality, Production, and customers to establish stable, capable, compliant manufacturing processes.

Supports Quality Engineering projects in a medical device micro-manufacturing environment under the guidance of a Quality Engineer. Responsibilities include line layout, process mapping, procedure and work-instruction drafting, fixture improvement and design, 5S and Lean Kaizen events, validation protocol execution, and project presentation and reporting.

Manufacturing Engineering Intern supporting process development, metrology, statistical analysis, tooling and fixture fabrication, manufacturing documentation, process validations, training materials, and continuous improvement initiatives under the guidance of a Manufacturing Engineer.

Develops and improves manufacturing processes for Nitinol tube and wire production. Responsibilities include creating routers, work instructions, flow charts, PFMEAs, control plans, and engineering documentation; troubleshooting production issues; supporting machine validation, operator training, lean initiatives, process controls, and continuous improvement; and partnering with Quality, Production, operators, and customers. The role also establishes manufacturing capacity, improves yields, supports cost reduction, and applies statistical methods such as DOE, SPC, and capability studies.

Partners with site leadership to implement HR strategies, including workforce planning, compensation, talent management, employee engagement, succession planning, recruitment, and training. Manages complex employee relations matters, investigations, compliance, performance management, and leadership coaching. Analyzes talent metrics and advises leaders on HR policies, employee development, and retention. This is an on-site role in Bethel, Connecticut, with travel up to 15%.

Supports ERP-based planning processes by maintaining item masters, BOMs, routings, work centers, and planning data. Assists with material planning, production scheduling, requirements gathering, system testing, issue resolution, reporting, documentation, and planner support. Participates in lean and continuous improvement initiatives across planning and procurement functions.

Leads enterprise excellence and continuous improvement initiatives across a medical device manufacturing site. Responsibilities include coaching Lean and Six Sigma practices, leading Kaizen and problem-solving activities, defining operational metrics, analyzing performance data, improving procedures, coordinating cross-site initiatives, and delivering cost savings. The role requires engineering expertise, Lean Black Belt certification, regulated-environment experience, knowledge of ISO quality systems, and occasional travel to other sites.

Develops and leads complex laser-based medical device product development projects from prototyping through production readiness. Responsibilities include process development, parameter optimization, troubleshooting, metrology programming, test method validation, engineering drawing interpretation, quality documentation, customer communication, quoting support, and cross-functional project leadership. The engineer also mentors technical staff, supports continuous improvement, and applies advanced manufacturing, materials science, and validation methods to high-precision medical device manufacturing.

Designs precision mechanical systems for laser micromachining and process manufacturing equipment. Creates SolidWorks models, assemblies, drawings, and BOMs; performs tolerance analysis, material selection, and manufacturability assessments. Integrates lasers, optics, motion systems, automation, controls, and machine vision. Coordinates with electrical, software, manufacturing, and suppliers; oversees prototypes, quality, compliance, and design optimization. Leads projects, delegates work, and mentors junior engineers.