Manufacturing Engineer - Level I

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 Engineering, Level 1 will be responsible for direct technical support for Instruments and Consumable Manufacturing operations in ISO 13485 and FDA regulated medical device setting. Representing Operations in design teams for new and on market product design and development, design transfer, and market phases. Facilitating in the definition of project tasks, establishing timelines, and fulfilling responsibilities for product design transfer and related process engineering. Collaborating on the development and assuming full ownership at Production release of material specifications/drawings, manufacturing processes, repair/refurb processes, fixtures, test methods, analysis tools, and related acceptance criteria for new or on market product. Leading and assisting in product, supplier, and process sustaining engineering initiatives to scale manufacturing throughput and improve quality, compliance, safety, yields, efficiency, reliability, and cost. 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.

Key Duties and Responsibilities

Represent Operations in design teams; fulfill design transfer responsibilities for new and on market product development, validation, and market release phases.

Assume full ownership of sustaining engineering support for on-market products

Lead or assist in sustaining engineering initiatives to support obsolescence management.

Lead or assist in product, supplier, and process sustaining engineering initiatives to improve quality, compliance, safety, efficiency, reliability, cost, and scale throughput.

Provide technical support for supplier issues

Participate and drive development and implementation of process automation strategies and solutions

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

Collaborate with R&D on development and assume full design transfer ownership for Production and Market release of material specifications/drawings, manufacturing processes, repair/refurb processes, fixtures, test methods, analysis tools, work instructions and related acceptance criteria for new or on market product.

Establish and maintain standard architecture of BOMs and routings

Collaborate with R&D on OQ process validation planning and execution. Assume full ownership of PQ process validation planning, execution, and reporting.

Assume full ownership of equipment, test fixture, test method, analysis tool validation planning, execution, and reporting; collaborate with R&D as required.

Ensure effective training of Manufacturing and Quality Control personnel for transfer of new processes.

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

Participate in or conduct applicable departmental, interdepartmental and intra-departmental training.

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.

Education, Experience, and Qualifications

Bachelor's Degree Bachelors of Science in the field of Mechanical, Electrical, Industrial, Bio-medical, or Biomechanical Engineering. required

5+ Years Experience and technical leadership supporting process improvement and sustaining engineering in a ISO 13485 and/or FDA regulated Life Sciences, Medical Device, or Medical Technology industry. preferred

1+ Years Experience working independently or as a team member in a fast-paced environment with rapidly changing priorities preferred

Thorough knowledge of ISO 13485 and FDA Quality System requirements

Knowledge of Enterprise Resource Planning, including applied knowledge of engineering functionality

Proficiency in the use of Product Lifecycle Management, including applied knowledge of Engineering Change Control

Applied knowledge of Process and Test Method Validations as required by FDA Quality System guidelines

Knowledge of Design Control requirements as defined by the FDA Quality System guidelines

Proven results through application of Six Sigma and Lean Manufacturing principles, including applied knowledge of statistical design of experiments

Mathematics and statistics aptitude.

Data analysis and technical writing aptitude.

Excellent oral and written communication skills.

Proficient in Microsoft Word, Excel, and PowerPoint programs.

Highly organized with proven time management and prioritization skills

Ability to work independently and with minimal supervision

Ability to handle the pressure of meeting tight deadlines

Standard Working Conditions

Work is typically performed in an office environment. - Frequently

Possible exposure to mechanical, biological, and chemical hazards. - Frequently

Possible exposure to Chemicals, Lasers, Excessive Noise, etc. - Frequently

Work in manufacturing setting which may include BioSafety Level 2 areas; work may be performed in fume hood, clean hood, biosafety cabinet, and/or ISO Class 7 cleanroom with specialized gowning and safety requirements - Frequently

Work in walk-in refrigerators and freezers that encompass conditions down to -20°C - Frequently

Travel Requirements

Travel may be required at least 10% of the time

What we offer

Receive a competitive salary and benefits package as you grow your career at DiaSorin. Join our team and discover how your work can impact the lives of people all over the world.

Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

Diasorin is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, protected veteran status, or any other characteristic protected by applicable law.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact [email protected] .

​Recruitment Fraud Notice

Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact [email protected] for verification.

Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.