Engineering Manufacturing jobs in Middlesex

The Product Lifecycle Engineer will be responsible for managing product lines throughout their entire lifecycle. You will collaborate with teams across R&D, Quality, Regulatory, and Manufacturing to support regulatory submissions, maintain market compliance, and develop engineering solutions that enhance the safety, quality, and performance of medical devices across various classifications.

The Electronic Engineering Supervisor is responsible for overseeing a team of electronic engineers engaged in the design, development, testing, and maintenance of electronic systems and components.

The Quality Manager role involves leading quality assurance and control functions across multiple manufacturing facilities, ensuring compliance with standards like ISO9001 and AS9100. The position emphasizes developing quality systems, managing supplier quality, and driving Total Quality Management initiatives while collaborating with internal and external stakeholders​.

The Quality Manager, indsutrial manufacturing, will provide leadership and management of quality assurance and control functions across multiple manufacturing facilities, ensuring compliance with industry standards and customer requirements. They will drive continuous improvement initiatives, oversee supplier quality programs, and maintain robust systems to support operational excellence and customer satisfaction at their Burlington, MA facility.

As the Systems Engineer, you will be tasked with tasks that will contribute to the development of cutting-edge medical technology and advancements. You will design and develop solutions for hardware and software components for impactful medical devices.

As the Manufacturing Engineer, you will have the exciting opportunity to develop life saving medical devices that will improve the lives of patients and help them take back their independence. You will contribute to prototyping and engineering activities that will directly impact the innovation of these devices.

As the Product Engineer, you will be oversee the entire product lifecycle of key product lines for this well known medical device company. Working closely with cross functional teams, you will develop solutions to improve medical devices to deliver exceptional products to the customer.

The Senior Software Quality Engineer is responsible for ensuring product quality during the software development life cycle, involving design, verification, and validation processes. Candidates should have at least eight years of experience in quality engineering within regulated industries, with knowledge of ISO standards and the ability to conduct risk management and internal audits.

My client is seeking a Manufacturing Engineer to play a key role in developing next-generation cardiology devices. You will oversee manufacturing processes, support early-stage production builds, and collaborate with cross-functional teams to ensure the efficient production of life-saving medical devices.

Manage & schedule shop floor departments (CNC/Polish/Inspection/Cutter Grind) to achieve quality, delivery and profitability, follow company rules and regulations, and maintain the schedule provided by the Manufacturing Manager or Production Control Supervisor.

As a Senior Manufacturing Engineer you will be taking on a variety of roles to meet the needs of an evolving product and company. You will be responsible for driving excellence in production processes, ensuring the delivery of high-quality, life-saving medical devices.

The Design Quality Engineer will play a critical role in ensuring that medical devices meet regulatory and quality standards throughout the product development lifecycle. This position involves collaborating with cross-functional teams to identify design risks, implement process improvements, and maintain compliance with ISO and FDA regulations.

My client is seeking an experienced engineer to support the development and manufacturing of innovative medical devices, with a focus on hands-on work in a cleanroom environment and leading process validation activities. The role involves collaborating with production teams, developing manufacturing processes, and working with external partners to scale up production.

The Production Manager will be responsible for the day today production floor, creating lean initiatives through developing processes and overseeing a team of direct reports.

This role focuses on supporting product development and manufacturing processes to ensure compliance with medical device quality standards. Key responsibilities include working with cross-functional teams to maintain compliance with FDA and ISO regulations, overseeing design controls, risk management, and verification/validation activities, and ensuring that product designs meet stringent quality and safety standards.

The Quality Manager will oversee all QA and Test personnel, ensuring the daily operation of the QA department runs smoothly and efficiently. They will also provide quality-related order correspondence to customers, staff and train the team, and prioritize daily tasks to ensure consistency and meet customer deliverables.

The Quality Manager will oversee our ISO 9001 and ISO 13485 certified quality system, managing daily quality operations and the inspection department at our CNC Manufacturing Facility. This role involves representing quality in company meetings and serving as a liaison with customers to address quality-related issues at our Belmont, MA site.

A leading general contractor specializing in a diverse pipeline of projects is urgently looking for a Project Manager to join their team for projects throughout Massachusetts and Nothern New England.

The Quality Manager will lead the development and implementation of quality control processes, ensuring compliance with regulatory standards while driving continuous improvement initiatives within the organization. This role involves managing the quality assurance team, conducting audits, and collaborating with cross-functional teams to enhance product quality and operational efficiency.

The Quality Manager is responsible for overseeing all aspects of the inspection process, including performing inspections, managing the calibration system, and leading a team of inspectors while fostering continuous improvement and quality standards. Additionally, the manager acts as a liaison with customers regarding quality issues, collaborates on inspection plans, and ensures effective communication and documentation throughout the department.

The Principal Powder Processing Engineer will design and implement key components for battery manufacturing, focusing on dry bulk powder handling and mixing systems. This role involves optimizing processes and collaborating with internal teams and suppliers to ensure project success in a fast-paced start-up environment.

The Automation Engineer will be responsible for automating, developing and implementing specific practices throughout the project time line through development and into manufacturing.

The Process Equipment Engineer will be the lead process engineer for one of the most impressive and well designed battery manufacturer in the Northeast.

The Manufacturing Supervisor is responsible for overseeing and coordinating the production activities within a manufacturing facility. The primary role is to ensure that production processes run smoothly, efficiently, and safely to meet production targets and quality standards.

The Engineering Technician is responsible for designing, building, and maintaining process equipment, with a focus on improving Precision Coating's Ion Implanter and IBAD equipment. Key tasks include upgrading high vacuum systems, developing automated manufacturing processes, troubleshooting complex electro-mechanical issues, and training personnel on equipment operation.

The Optical Field Service and Operations Technician is responsible for installing, troubleshooting, and maintaining advanced optical and fiber-optic systems at customer sites, ensuring optimal performance and minimal downtime. The role combines hands-on technical work with strong customer service skills, requiring travel to various locations and adherence to industry standards and safety protocols.

The Senior Manufacturing Engineering Leader will oversee the development and optimization of manufacturing processes for laser medical equipment, focusing on enhancing production efficiency, product quality, and cost-effectiveness. This role involves leading continuous improvement initiatives, mentoring junior engineers, and ensuring compliance with quality and safety standards in a fast-paced manufacturing environment.

The Quality Manager will oversee the quality management system in a precision manufacturing environment, leading the inspection department and managing direct reports such as inspectors and quality engineers. This role involves fostering a collaborative work culture while driving continuous improvement initiatives, implementing ISO standards, and maintaining strong communication with customers and management to effectively resolve quality-related issues.

This role involves installing, configuring, and maintaining fiber-optic networks and equipment, ensuring optimal performance through troubleshooting and upgrades. The technician will also provide exceptional customer support and documentation while adhering to safety and compliance standards.

The NPI Engineer will be vital in designing and developing new medical devices. Key responsibilities include creating assembly and test fixtures, assisting with validation studies, and optimizing processes. The engineer will ensure compliance with industry standards, contribute to manufacturing instructions, and provide training on assembly processes. The role also involves collaborating with cross-functional teams, troubleshooting complex issues, and understanding materials science relevant to medical devices.