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, we've 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 that's 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 you're passionate about innovation, diversity, and making a positive impact on healthcare, Diasorin is the place for you. We're 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 that's 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!

Job Scope

This position will be responsible for participating in the company's day to day Reasearch & Development activities which include design, execution and interpretation of scientific experiments and design and development of assays based on Luminex's technology platform and chemistries. Handles scientific experiments independently with minimal supervision.

Key Duties and Responsibilities

Day-to-day “hands on” work in the laboratory including, planning and designing of experiments, generating, recording, and analyzing experimental data and maintaining laboratory notebooks. This involves working in Biosafety Level II laboratory with biological samples and nucleic acid extractions.

Routinely, assemble and present data to departmental, project, and cross-site teams

Significantly contribute to writing protocols and reports relating to feasibility, verification and validation of molecular tests under quality system requirements

Interface across the organization and work closely with other functional groups, such as, Quality Affairs, Regulatory Affairs, Clinical Affairs, Design Transfer, Manufacturing, and Quality Control regarding priorities and timetables for deliverables

Provide training and technical support to junior members of the team

Assist in intellectual property development

Conform to applicable Design Control regulations and standards

Troubleshoot technical difficulties, as required

Comply with the company quality policies and operating procedures

Participate in the maintenance of general laboratory organization

Performs other duties as assigned related to duties as assigned

Education, Experience, and Qualifications

Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field combined with at least 5 years’ laboratory work experience in molecular biology or the biotechnology industry required or

Bachelor's Degree Bachelor degree in biological/chemical or related scientific disciplines with 2 years relevant experience/training preferred or

Master's Degree Master’s degree in biological/chemical or related scientific disciplines with no relevant experience/training preferred or

2+ Years Expertise in a variety of molecular and biochemical laboratory procedures required

2+ Years Knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation required

2+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred

2+ Years Prior medical device industry experience preferred

Excellent oral and written communication skills. (High proficiency)

Proficient in Microsoft Word, Excel, and PowerPoint programs. (High proficiency)

Highly organized with proven time management and prioritization skills (High proficiency)

Ability to work independently and with minimal supervision (High proficiency)

Ability to handle the pressure of meeting tight deadlines (High proficiency)

Excellent interpersonal skills with proven ability to work both in a team-oriented environment and independently (High proficiency)

Knowledge of Design Control requirements as defined by the FDA Quality System guidelines (Medium proficiency)

Mathematics and statistics aptitude. (Medium proficiency)

Data analysis and technical writing aptitude. (Medium proficiency)

What we offer
The hiring range for this position is $57,738 - $98,155 annually. The salary range for this role represents the numerous factors considered in the hiring decisions including, but not limited to, educations, skills, work experience, certifications, etc. Beyond base salary, Diasorin offers a competitive rewards package focused on your overall well-being. We are proud to offer a comprehensive plan of health benefits, retirement and financial wellbeing, time off programs, wellbeing support and perks. Benefits may vary by role, country, region, union status, and other employment status factors. You may also be eligible to participate in an annual incentive program. An incentive award, if any, depends on various factors, including, individual and organizational performance.

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 hrtalent@diasorin.com or 1-800-328-1482 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.