Engineering Manufacturing jobs in Middlesex

The Process Engineering team is seeking a talented and passionate process engineer to grow and establish a team of engineers to work on several new product lines in their new facility.

As the Product Lifecycle 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 Quality Engineers primary responsibility for this position is to be hands on with the day to day quality-related issues within the various production operations. Additionally, you will be helping drive improvements and provide support cross departmentally to improve overall product quality.

The Quality Manager is responsible for ensuring the highest quality standards across the production life cycle, overseeing QA and testing personnel, and providing quality-related correspondence to customers. You will also upholds safety, ITAR compliance, and organizational communication standards while contributing to strategic policy formulation and company goal setting.

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.

In this role, you will develop and maintain quality systems and procedures, including inspection plans and statistical analyses, to ensure product and process standards are met. Additionally, you will collaborate with cross-functional teams to address quality issues and drive continuous improvement initiatives.

I'm seeking a Process Engineer to design, optimize, and implement manufacturing processes that deliver high-quality renewable energy equipment efficiently and sustainably. The ideal candidate will combine technical expertise with a passion for renewable energy to drive process improvements and contribute to the success of operations.

The Production Supervisor will oversee and improve safety, quality, cost, delivery, and team morale within the production area, leading a team of up to 50 employees. The role involves driving continuous improvement, ensuring compliance with safety and quality standards, and supporting the company's overall strategy through leadership and cross-functional collaboration.

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.

This position will manage, design, and implement engineering solutions to optimize production processes, improve efficiency, and ensure product quality. It will also implement solutions to enhance the overall manufacturing process, identifying areas for improvement and collaborating closely with cross-functional teams.

The Quality Engineer (engineering materials / industrial manufacturing) will manage quality operations within the assigned Value Stream, ensuring products and processes meet established standards and driving quality improvement initiatives. They will gather and analyze data to support root cause analysis, implement corrective actions, and achieve plant quality objectives in alignment with the Corporate Strategy.

The Process Engineer will contribute to technology industrialization, process optimization, equipment design, and operational support. This hands-on role involves pilot equipment operation, process development, and data documentation, while fostering innovation, collaboration, and transparency.

The Product Life-cycle Engineer will manage and sustain medical device product lines throughout their life-cycle, collaborating with cross-functional teams to ensure compliance, quality, and safety. The role involves conducting gap assessments, leading design and process improvements, and ensuring regulatory compliance while maintaining strong partnerships across the organization.

The Senior Quality Engineer, Medical Device Software, will lead quality assurance activities throughout the product development lifecycle, focusing on new product development for complex medical devices. This role requires expertise in design controls, risk management, and regulatory compliance, with a strong emphasis on collaboration across engineering teams to ensure high-quality, patient-specific solutions at our Bedford, MA facility.

The Quality Engineer II involves managing quality operations for specific value streams by developing and maintaining quality standards, systems, and procedures. Key responsibilities include conducting statistical analyses, driving continuous improvement initiatives, ensuring compliance with industry standards (e.g., ISO9001, AS9100), and collaborating with customers, suppliers, and internal teams to enhance product and process quality.

The Senior Manufacturing Engineer will join a small team reporting directly into the Vice President. This person will wear several hats, with responsibilities including supplier management, hands-on assembly, cleanroom operations, NPI efforts, test and process validations, and sterilizations.

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​.

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.

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 Mechanical Engineer will be responsible for providing technical expertise in the design and development of innovative consumer products. The ideal candidate will have a strong background in mechanical engineering, with a focus on product development and Mandarin language proficiency.