Job Description

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!ASSOCIATE SCIENTIST I - AGS - CAJob PostingOur MissionWe envision a Luminex solution in every lab around the world seeking to obtain timely and confident answers.Our VisionWe aim to lead with transformative solutions that uniquely accelerate reliable answers while reducing the overall cost of advancing health.A Brief OverviewParticipate in the Company's day-to-day Research and Development activities which include: design, execution and interpretation of scientific experiments and design and development of sequencing, fragment analysis and other molecular assays. The position will carry out scientific experiments independently with supervision from senior members of the team.What you will do

• Day-to-day hands on work in the laboratory including generating, recording, and analyzing experimental data and maintaining records

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

• 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, Regulatory Affairs, Clinical Affairs, Assay R&D, and Quality Assurance regarding priorities and timetables for deliverables

• Assist in intellectual property development

• Conform to applicable Design Control regulations and standards

• Troubleshoot technical difficulties, as required

• Comply with the Company's quality policies and operating procedures

• Participate in the maintenance of general laboratory organization

• Other duties as assigned.

Education Qualifications

• Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field combined with at least 2 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 preferred

Experience Qualifications

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

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

• 1+ Years Theoretical and technical competency with Sanger sequencing, Next-Generation-Sequencing, digital PCR and real-time PCR preferred

• 1+ Years Knowledge and competency with Containment Level 2 (CL2) procedures and requirements preferred

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

• 1+ Years Prior medical device industry experience preferred

Training and Skills

• Excellent oral and written communication skills (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 (Low proficiency)

• Mathematics and statistics aptitude (Medium proficiency)

• Data analysis and technical writing aptitude (Medium proficiency)

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

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

• Ability to work independently and with minimal supervision (Medium proficiency)

Travel Requirements

• 10%

Luminex Corporation is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, age, national origin, disability status of an otherwise qualified individual, citizenship status, membership or application for membership in a uniformed service, or any other protected characteristic or category protected by applicable law.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 1-800-328-1482 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.

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