Quality Engineer

Diasorin is a global leader in diagnostic solutions pushing the boundaries of science and technology to create cutting-edge tools that improve healthcare worldwide. With a legacy spanning over 50 years weve earned our reputation for excellence by developing innovative diagnostic assays and instruments that are trusted by healthcare providers around the world.

Our broad offering of diagnostic tests and Licensed Technology solutions made available thanks to ongoing investments in research positions us as the player with the widest range of specialty solutions in the sector and identifies us as the Diagnostics Specialist.

Why Join Diasorin

• Impactful Work: When you join Diasorin you become part of a team thats dedicated to improving lives. Your contributions will directly impact patient care making a meaningful difference in the world.

• Global Reach & Innovation: Our work transcends borders. Joining Diasorin means collaborating with colleagues from all over the world expanding your horizons and contributing to global healthcare solutions at the forefront of the diagnostic industry.

Diverse and Inclusive Culture: We believe in the strength of diversity and our inclusive culture reflects this commitment. We value your unique perspective and offer a supportive collaborative environment where everyone can thrive.

Join Our Team: If youre passionate about innovation diversity and making a positive impact on healthcare Diasorin is the place for you. Were looking for passionate and talented individuals who are ready to embrace new challenges and drive healthcare solutions forward.

Are you ready to be part of a dynamic team thats shaping the future of diagnostics Join Diasorin and become a catalyst for change in the world of healthcare. Apply today and be a part of our exciting journey toward a healthier more connected world. Together we can make an impact!

SUMMARY

Responsible for evaluating and optimizing manufacturing QC R&D and CAPA processes to improve product consistency and to increase productivity. Responsible for reviewing performing and documenting validations for new and existing products. Supports all applicable regulations including but not limited to FDA ISO IVDD and IVDR requirements.

ESSENTIAL DUTIES & RESPONSIBILITIES

Review of design manufacturing purchasing and test documentation to ensure quality requirements are fulfilled.

Review specifications operation instructions sheets process procedures test procedures inspection and test analysis.

Provide leadership in and employ advanced quality planning techniques (FMEA Capability Studies Measuring and Test Equipment Studies Product Validation and Reliability Test)

Assist in determining process/equipment capabilities.

Assist in the development process flow diagrams and perform gap analyses on current controls versus required controls.

Investigate the root cause of external and internal non-conforming products.

Assist in corrective and preventive actions and verifications of effectiveness such as actions for customer complaints internal audits and internal and external suppliers non-conformance.

Perform assessments for process-related risks.

Assist in the development of inspection procedures and justified sample plans.

Gather analyze and report data reflecting status of product and process and provide recommendation to improve.

Support new product development and growth. Represent quality on new product development teams with guidance from more senior quality engineers or management.

Participate in improvement and lean projects.

Performs internal audits

Responsible for performing assigned tasks in accordance with the companys quality policies and procedures per the applicable quality management system regulations as defined in the Quality Manual.

Responsible for performing assigned tasks in accordance with applicable Environmental Health and Safety (EHS) regulations and Company EHS policies. Violations of EHS regulations or policies will be handled in accordance with the established Company disciplinary process.

Perform other duties as assigned

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 or protected veteran status and will not be discriminated against on the basis of disability.

In compliance with federal law all persons hired will be required to verify identity and eligibility to work in the United States and Canada and to complete the required employment eligibility verification document form upon hire.

Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities. If you are a US or Canada candidate and require assistance or accommodation during the application process please contact the North America Talent Acquisition Team at or 1- to request an accommodation.

The above job description is intended to describe the general content identify the essential functions and set forth the requirements for the performance of this job. It is not to be construed as an exhaustive statement of duties responsibilities or requirements.

Diasorin reserves the right to modify or amend this job posting as needed to comply with local laws and regulations.

Please note that offers of employment at Diasorin may be contingent upon successful completion of a pre-employment background check and drug screen subject to applicable laws and regulations.

This position is not eligible for partnership with a third-party search firm vendor without expressed written consent from the Diasorin Human Resources Department.