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About the Role

As the Diagnostics Specialist, you will participate in the company's day-to-day research activities, including designing, executing, and interpreting scientific experiments and developing assays using Luminex's technology platform. You will conduct scientific experiments independently with supervision from senior team members, contributing to solutions that improve patient care worldwide in an entrepreneurial and collaborative global environment.

Responsibilities

Perform day-to-day laboratory work, including generating, recording, and analyzing experimental data.
Maintain laboratory notebooks and work in a Biosafety Level II laboratory with biological samples and nucleic acid extractions.
Assemble and present data to departmental, project, and cross-site teams.
Contribute to writing protocols and reports for feasibility, verification, and validation of molecular tests under quality system requirements.
Interface across the organization and collaborate with functional groups such as Clinical Affairs, Design Transfer, Manufacturing, and Quality Control.
Assist in intellectual property development.
Conform to applicable Design Control regulations and standards.
Troubleshoot technical difficulties.
Comply with company quality policies and operating procedures.
Participate in the maintenance of general laboratory organization.
Perform other duties as assigned.

Requirements

Associate's Degree in biochemistry, biology, molecular biology, or a related scientific field with at least 2 years of laboratory work experience in molecular biology or the biotechnology industry.
Bachelor's Degree in biological/chemical or related scientific disciplines with 1+ years of expertise in molecular and biochemical laboratory procedures.
1+ Years of knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation.
1+ Years of working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred.
1+ Years of prior medical device industry experience preferred.

Skills

Excellent oral and written communication skills.
Ability to handle the pressure of meeting tight deadlines.
Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently.
Knowledge of Design Control requirements as defined by the FDA Quality System guidelines.
Mathematics and statistical aptitude.
Data analysis and technical writing aptitude.
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.

Location

Domestic

Work Type

Full-time
Onsite

Experience Level

2+ years laboratory work experience
1+ Years Expertise
1+ Years Knowledge
1+ Years Working knowledge or experience
1+ Years Prior medical device industry experience

Education Level

Associate's Degree
Bachelor's Degree

Benefits

Competitive rewards package focused on your overall well-being.
Comprehensive plan of health benefits.
Retirement and financial wellbeing.
Time off programs.
Wellbeing support and perks.
Potential eligibility for an annual incentive program.

About the Company

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide.
For more than 50 years, Diasorin has combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results.
Diasorin continuously invests in research, technology, and people, guided by values of operational excellence, customer focus, and teamwork.
Diasorin empowers teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.
Diasorin is committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers.
Diasorin believes diverse perspectives strengthen innovation and help deliver meaningful impact for patients and customers worldwide.

Equal Opportunity

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.