Manufacturing Engineer - Level II

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry's broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

* Build What Matters

Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.

* Innovate with Agility at a Global Scale

Work in an entrepreneurial environment that enables speed, collaboration, and global impact.

* Grow in a People-Centered Culture

Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

The Manufacturing Engineer, Level II will be responsible for: designing, developing, and implementing automated control systems to enhance the efficiency and reliability of our Instruments Manufacturing operations. This role requires a strong technical background, attention to detail, and a deep understanding of automation and control systems in a regulated environment (ISO 13485 and FDA regulated medical device setting). Facilitating in the definition of project tasks, establishing timelines, and fulfilling responsibilities for product design transfer and related process engineering.

Facilitating the investigation and resolution of findings identified through audits, non-conformances, corrective/preventative actions, or customer complaints. Task-specific and change control training of Manufacturing personnel.

Job Duties and Responsibilities

* Design, develop, and implement control systems for automation in the manufacturing of medical devices.

* Develop and program PLCs (Programmable Logic Controllers) and/or HMI (Human-Machine Interface) systems.

* Collaborate with R&D, Quality Assurance, and Manufacturing teams to identify automation needs and develop solutions.

* Troubleshoot and resolve control system issues to ensure optimal performance and reliability.

* Ensure compliance with regulatory standards (e.g., FDA, ISO 13485) in the design and implementation of control systems.

* Develop and maintain detailed documentation of control systems, including schematics, wiring diagrams, and software code.

* Conduct risk assessments and participate in Failure Modes and Effects Analysis (FMEA) to identify and mitigate potential issues.

* Assume full ownership of design, specification development and selection of new production equipment, such as, test fixtures, manufacturing aids, and automation equipment; includes scale-up of existing processes and development of new processes

* Stay updated on industry trends, standards, and technological advancements to continuously improve automation processes.

* Lead and assist in engineering change control and document change control activities; participate in change control reviews.

* Ensure effective training of Manufacturing and Quality Control personnel for transfer of new test fixtures, manufacturing aids, and automation equipment

* Assist the investigation and resolution of findings impacting the organization identified through audits, non-conformances, corrective/preventative actions, or customer complaint escalation.

* Lead and assist in design input and implementation oversight of infrastructure improvement projects

* Lead and assist external technology transfers and contract manufacturing transfers.

* Ensure personal compliance and promote operational compliance with the Quality System and other regulations.

* Ensure compliance to NFPA, OSHA, lock-out, and other applicable safety standards.

* Other duties as assigned.

Education and Experience Qualifications

* Bachelor's degree in relevant engineering discipline; electrical, automation, or process control preferred.

* Bachelor's degree in Electrical Engineering, Mechanical Engineering, Automation Engineering, or a related field.

* 2+ years of experience in control/automation engineering, preferably in the medical device or a similar regulated industry.

* Proficiency in programming and configuring HMI systems.

* Data analytics experience (SQL, Tableau, Power BI)

* Experience programming in Python (Scripting and Automation)

* Advanced user of Solid Works

* Excellent problem-solving skills and attention to detail.

* Strong communication and teamwork skills.

* Experience with SCADA systems and industrial networks

* Equipment integration experience using IIoT, OPC and/or PTC Kepware

* Ability to debug…