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This Quality Manager will oversee the full Quality Management System, support new product development, and drive continuous improvement across a diverse manufacturing environment. They'll serve as the primary quality liaison for customers while ensuring smooth production, timely problem resolution, and operational excellence.
The Senior Quality & Regulatory Engineer will serve as the primary U.S. quality lead for Class II spine medical devices, ensuring regulatory compliance and seamless oversight of international manufacturing partners. The role offers autonomy, strategic influence, and direct interaction with FDA, suppliers, and global engineering teams.
The Quality Manager oversees the Quality Management System, new product development quality, and continuous improvement initiatives in a fast‑paced manufacturing environment. The position is highly hands‑on, blending technical problem solving with leadership responsibilities across engineering, operations, and customer engagement.
This is a high‑impact, hands‑on manufacturing engineering position supporting the scale‑up and ongoing production of next‑generation medical device assemblies. The Lead Manufacturing Engineer will develop, refine, and validate manufacturing processes; build fixtures and tooling; improve assembly workflows; and ensure production readiness by partnering closely with quality, operations, and engineering teams.
This role ensures products and manufacturing processes meet strict quality, regulatory, and customer standards while supporting audits, inspections, and continuous improvement. It also leads root‑cause investigations, manages non‑conformances and FAIRs, and partners with production teams to strengthen overall quality performance
This role serves as the U.S.-based quality and regulatory lead, ensuring full compliance with medical‑device regulations while overseeing quality systems, supplier performance, and imported product controls. It supports audits, design transfer, CAPA, inspections, and end‑to‑end oversight of global manufacturing partners to maintain product safety, documentation accuracy, and regulatory readiness.
This role supports production and customer quality by maintaining and improving the quality management system, driving process controls across front‑end and back‑end manufacturing, and leading cross‑functional problem‑solving for continuous improvement. It oversees CAPA, audits, supplier quality, risk assessment, validation activities, and compliance with industry standards to ensure products meet strict regulatory and customer requirements.
Joining the Electrical Engineering team, the Electrical Test Engineer II will play a key part in ensuring the performance, reliability, and quality of advanced hardware and embedded firmware systems. You will work cross-functionally to build automated test strategies, troubleshoot complex issues, and support continuous improvement throughout the development lifecycle.
My client is seeking a Product Development Engineer to support next‑generation power conversion solutions. This role offers hands‑on involvement with innovative products, advanced engineering challenges, and opportunities to influence system‑level designs used by major industry leaders.
The Engineering Manager blends hands-on technical work with team leadership. The role focuses on maintaining product compliance across Class I-III devices through updated test protocols, documentation, and design changes. You'll work closely with internal partners to ensure standards are kept current, gaps are identified early, and products continue to meet regulatory and customer expectations.
This role supports production by ensuring materials and processes meet customer specifications. It also resolves metallurgical issues and improves processing methods.
The Manufacturing Engineer focuses on developing and optimizing CNC machining processes for high-precision orthopedic implants and instruments.The position offers hands-on involvement from programming and fixturing through first-article production and continuous improvement.
The Manufacturing Engineer is responsible for developing and optimizing manufacturing methods, tooling, and documented processes to improve efficiency and product quality. This role involves analyzing production challenges, supporting CAD/CAM activities, collaborating with supervisors, and ensuring adherence to technical specifications, safety standards, and continuous improvement initiatives.
Supports materials, metallurgy, and surface‑engineering operations. Hands‑on work in coatings, heat‑treating, metallography, customer interaction, and process development while growing under an experienced metallurgist.
The Engineering Program Manager is responsible for leading the planning, execution, and successful delivery of complex programs that involve chemical processes, metallurgical systems, and electrochemical technologies. The Program Manager will guide new product and process development from concept through commercialization, ensuring technical rigor, high quality, and on-time delivery.
This role supports the development and manufacturing of biologic medical devices, focusing on implantable biologic materials. Responsibilities include new product development, process engineering, analytical testing, and validating tissue‑processing steps. The position is highly technical and hands‑on, supporting both existing product lines and new biologic research initiatives.
Lead and inspire a team of Product Life Cycle Engineers while driving cutting‑edge testing, compliance, and design improvements that keep advanced Class I-III medical devices at the forefront of global standards. As a cross‑functional force‑multiplier, you'll shape product strategy, elevate quality, fuel innovation, and ensure every device delivers exceptional performance and unmistakable customer value.
This role oversees safety programs, regulatory compliance, and facility operations to ensure a secure, efficient, and well‑maintained workplace. It combines strategic planning with hands‑on leadership across environmental, health, safety, and facilities functions.
We are seeking a highly experienced Principal Engineer with a strong background in medical device engineering to lead critical initiatives across both new product development (NPD) and post‑market sustaining engineering. This role will play a key part in ensuring product performance, safety, compliance, and continuous improvement across a diverse portfolio of Class I, II, and III medical devices.
This position focuses on testing, validating, and improving sophisticated hardware and embedded firmware systems. The role includes test planning, automation development, firmware debugging, hardware integration testing, and cross‑functional collaboration. You'll work closely with hardware and firmware teams to ensure products meet performance, reliability, and quality standards.
This role supports manufacturing operations by analyzing processes, driving continuous improvement initiatives, and implementing sustainable Lean methodologies. You will deliver data‑driven insights, improve cycle time and efficiency, and guide cross‑functional teams through structured improvement efforts.
This Operational Excellence Engineer role focuses on analyzing, designing, and improving manufacturing and business processes to boost overall operational efficiency. You'll partner closely with cross‑functional teams to deliver measurable improvements in cycle time, productivity, cost, and quality.
The Operational Excellence Manager leads all quality, continuous improvement, safety, and process engineering functions across the operation. You'll partner closely with senior leadership to elevate performance, develop strong teams, and drive world‑class operational rigor.
Develop advanced voltage regulator systems through hands‑on design, simulation, prototyping, and system‑level validation. Close collaboration with customers and internal engineering team and optimize next‑generation power conversion technologies.
The Senior Manufacturing Engineer supports the manufacturing and scale‑up of complex medical device components and assemblies. The engineer will collaborate closely with cross‑functional teams to refine processes, improve manufacturability, and ensure consistent, high‑quality output. It's a hands‑on position focused on assembly engineering, process documentation, quality compliance, and floor support within a regulated environment.
This role leads quality, continuous improvement, safety, and process‑engineering initiatives to drive world‑class operational performance across the organization. It oversees daily SQDCI activities, manages quality and materials functions, and guides company‑wide OpEx efforts - including kaizen events, supplier‑process improvements, cost‑out projects, and performance tracking.
This role leads environmental, health, safety, and facilities functions by developing compliant EHS programs, conducting audits and risk assessments, and overseeing incident investigations and training to maintain a safe, efficient workplace. It also manages facilities operations, contractors, capital projects, and maintenance activities while driving continuous improvement and ensuring regulatory alignment across all site functions.
The General Manager will oversee onsite operations and guide the company through significant growth. With a team of approximately 15 employees and increasing revenue, the business is primed for scale. This leader will strengthen operations, rebuild customer engagement, and position the organization for sustained success. This is a fully onsite role with high visibility and substantial decision-making authority.
A hands-on operational leader is needed to oversee daily production, strengthen core processes, and drive organizational alignment within a specialized precision manufacturing environment. This position is responsible for optimizing workflows, improving quality structures, enhancing communication across functions, and setting the tone for culture and accountability. The role also plays a key part in reestablishing and growing customer relationships to support long‑term expansion.
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