Medical Devices jobs

The Project Engineer leads efforts in medical device development and manufacturing, making sure projects meet quality, budget, and timeline goals. This role involves both hands-on design work and project management skills in a regulated environment.

The Facilities Manager will oversee the maintenance and efficient operation of a multi-site manufacturing facility, ensuring compliance, safety, and reliability. The Facilities Manager leads a team and manages vendor relationships while driving long-term strategies for equipment and infrastructure.

As a Senior Program Manager in the life science industry, you will oversee complex projects within the engineering and manufacturing department, ensuring their successful execution from initiation to completion. This role requires strong leadership and organizational skills to manage cross-functional teams.

The Facilities Manager will oversee the efficient operation, maintenance, and safety of facilities in the medical device industry. This role requires expertise in engineering and manufacturing processes to ensure optimal functionality and compliance while being able to manage a solid team of supervisors.

The CNC Swiss Lathe Programmer is responsible for interpreting a drawing and specifying the process, program and tooling required for production. Once blueprints are finalized and approved by management, the Programmer will set up the machines for production. The CNC Swiss Lathe Programmer is also responsible for leading the team of Machinists that will keep parts running without consultation to deliver low error, on-time results to the customer.

The Project Manager is a key contributor in driving medical device manufacturing and product development projects from concept to completion. In this role you will provide hands-on support for designs of components, evaluate processes and tooling, ensure accurate process documentation, and strengthen project execution.

The Project Manager role supports the end-to-end development and manufacturing of medical devices in a highly regulated environment.

The position blends project leadership, hands-on engineering, and compliance to drive successful product launches and process improvements.

The Supplier Quality Engineer role focuses on ensuring supplier compliance and driving quality improvements across the supply chain by conducting audits, managing corrective actions, and supporting new product development. It requires collaboration with internal teams and suppliers to maintain standards, reduce risks, and implement continuous improvement initiatives.

The Senior Regulatory Affairs Specialist is ideal for a regulatory professional ready to take the next step in their career and thrive in a dynamic, fast-paced environment. You will lead regulatory strategies and submissions for innovative medical devices, ensuring compliance with global requirements and supporting successful product approvals.

Reporting into the Site Lead, the Senior Manufacturing Manager will oversee and optimize manufacturing operations, ensuring efficient production processes and quality standards are consistently met. The Senior Manufacturing Manager will be responsible for optimizing resources to achieve safety, quality, schedule, and cost goals, while maintaining compliance with internal policies and external regulations - including environmental, OSHA, and FDA standards.

The Design Quality Engineer ensures that all medical device design and development activities meet safety, performance, and regulatory standards. This role partners with cross-functional teams to support new product development and sustaining engineering projects, driving quality, compliance, and risk management throughout the design lifecycle

The Quality Manager leads the company's Quality Systems in compliance with ISO 13485 and global medical device regulations, ensuring robust oversight of product release, CAPA, audits, and technical investigations. This role is critical in maintaining regulatory readiness and driving continuous improvement across the organization's quality operations.

The Supplier Quality Engineer will qualify and audit suppliers, validate new products, and ensure compliance with ISO 13485, AS9100, and ISO 9001 standards while supporting NPI projects and resolving supplier-related issues. They will also monitor supplier performance, drive corrective actions, and collaborate across teams to maintain quality and regulatory compliance throughout the global supply base.

As a Senior Program Manager in the life science industry, you will oversee complex projects within the engineering and manufacturing department, ensuring their successful execution from initiation to completion. This role requires strong leadership and organizational skills to manage cross-functional teams.

The Project Engineer/Manager leads and manages medical device product development and manufacturing transfer projects from concept through production. The position combines hands-on engineering design, regulatory compliance, and project management to deliver high-quality products in a fast-paced, startup-like environment.

The Quality Manager will oversee and continuously improve quality control systems, ensuring compliance with ISO 9001 and 13485 standards through detailed inspections, audits, and team training. They will lead efforts in quality assurance, non-conformance resolution, and customer satisfaction while supporting production teams with real-time inspection oversight and process enhancements.

A new product line is entering development, and my client needs a Quality Engineer to guide its design activities and ensure compliance throughout the process. This position will also take the lead in creating and organizing documentation for the company's quality systems and related programs. The employer is a specialized manufacturer that builds electro-mechanical solutions exclusively for the medical device industry

This position is responsible for managing quality systems, including audits, compliance with regulatory standards, and oversight of product release and corrective actions. The role requires strong leadership, regulatory knowledge, and experience in a highly regulated manufacturing environment.

The Quality Manager leads the company's Quality Systems in compliance with ISO 13485 and global medical device regulations, ensuring robust oversight of product release, CAPA, audits, and technical investigations. This role is critical in maintaining regulatory readiness and driving continuous improvement across the organization's quality operations.

The Senior Supplier Quality Engineer will play a critical role in ensuring supplier quality within the engineering and manufacturing department. This position requires a proactive approach to quality assurance and collaboration with suppliers in the business services industry.

The Senior Supplier Quality Engineer leads supplier quality strategy and execution, driving supplier development, corrective actions, and continuous improvement across a global medical device supply chain. The role works cross-functionally to qualify suppliers, support new product development, conduct audits, and ensure high-quality components for critical lifesaving technologies.

The Inside Sales Manager will lead and manage sales strategies within the Medical Device and Medical Manufacturing space. This role will be a player-coach position, working with your team and hitting your own sales goals.

A new product line is entering development, and my client needs a Quality Engineer to guide its design activities and ensure compliance throughout the process. This position will also take the lead in creating and organizing documentation for the company's quality systems and related programs. The employer is a specialized manufacturer that builds electro-mechanical solutions exclusively for the medical device industry

This role ensures that external suppliers consistently meet stringent quality, regulatory, and reliability requirements for complex medical devices. It involves leading supplier audits, driving corrective actions, and partnering closely with engineering and manufacturing to prevent issues before they reach patients.

Are you a detail-driven quality expert with a passion for precision manufacturing? Our client, a leading medical device contract manufacturer, is seeking a Quality Control Manager to lead inspection operations and uphold ISO standards in their state-of-the-art facility.

This is a QE or Senior QE opportunity (depending on experience) within the industrial & medical device manufacturing space - offering an opportunity to join a dynamic company in an environment that is fast paced, customer/quality focused, and engaging.

This is a quality manager position with a medical device component manufacturer in the north suburbs of Chicago. This role will oversee the metal component division, supporting high-profile customers in the industry.

This Manufacturing Engineer role focuses on improving production processes, supporting new product launches, and ensuring quality standards in a fast-paced manufacturing environment. Ideal candidates will bring 3+ years of experience-preferably in medical device or plastics-and be ready to contribute with minimal training.

This Manufacturing Engineer role focuses on improving production processes, supporting new product launches, and ensuring quality standards in a fast-paced manufacturing environment. Ideal candidates will bring 3+ years of experience-preferably in medical device or plastics-and be ready to contribute with minimal training.

Are you a Quality Engineer with Supplier experience? Do you have experience working in the Manufacturing industry (ideally Plastics, Medical Device, Electronics, Industrial Manufacturing)? Do you have ISO 13485 or ISO 9001 experience? Are you okay with traveling 10% of the time? If so, please read on and apply to the Supplier Quality Engineer - Plastics Manufacturing job based near Providence, RI.