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About the Role

This position will be responsible for participating in the company's day-to-day Research & Development activities, including the design, execution, and interpretation of scientific experiments, as well as the design and development of assays based on Luminex's technology platform and chemistries. The role requires handling scientific experiments independently with minimal supervision.

Responsibilities

• Perform day-to-day laboratory work, including planning and designing experiments, generating, recording, and analyzing experimental data, and maintaining laboratory notebooks.
• 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 other functional groups, such as Quality Affairs, Regulatory Affairs, Clinical Affairs, Design Transfer, Manufacturing, and Quality Control.
• Provide training and technical support to junior team members.
• 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 combined with at least 5 years of laboratory work experience in molecular biology or the biotechnology industry.
• Bachelor's Degree in biological/chemical or related scientific disciplines with 2 years relevant experience/training preferred.
• Master's Degree in biological/chemical or related scientific disciplines with no relevant experience/training preferred.
• 2+ Years of expertise in a variety of molecular and biochemical laboratory procedures.
• 2+ Years of knowledge of routine laboratory methods such as PCR, data analyses, specimen handling and processing, and experimental documentation.
• 2+ Years of working knowledge or experience with ISO 13485:2016 standards and FDA regulations preferred.
• 2+ Years of 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).

Skills

• Luminex technology platform
• Luminex chemistries
• PCR
• Data analysis
• Specimen handling and processing
• Experimental documentation
• ISO 13485:2016 standards
• FDA regulations
• Microsoft Word
• Microsoft Excel
• Microsoft PowerPoint
• Design Control requirements

Experience Level

• 5 years laboratory work experience in molecular biology or the biotechnology industry (with Associate's Degree)
• 2 years relevant experience/training (with Bachelor's Degree)
• No relevant experience/training (with Master's Degree)
• 2+ Years Expertise in molecular and biochemical laboratory procedures
• 2+ Years Knowledge of routine laboratory methods
• 2+ Years Working knowledge or experience with ISO 13485:2016 standards and FDA regulations
• 2+ Years Prior medical device industry experience

Education Level

• Associate's Degree Community College 2-year diploma (technical) in biochemistry, biology, molecular biology, or a related scientific field
• Bachelor's Degree in biological/chemical or related scientific disciplines
• Master's Degree in biological/chemical or related scientific disciplines

Salary/Compensations

• $57,738 - $98,155 annually

Benefits

• Competitive rewards package
• Comprehensive plan of health benefits
• Retirement and financial wellbeing programs
• Time off programs
• Wellbeing support and perks
• Potential eligibility for an annual incentive program

About the Company

• 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, Diasorin has earned its reputation for excellence by developing innovative diagnostic assays and instruments trusted by healthcare providers globally.
• The company's broad offering of diagnostic tests and Licensed Technology solutions, supported by ongoing investments in research, positions it as a key player with the widest range of specialty solutions in the sector, identifying it as the 'Diagnostics Specialist.'
• Diasorin offers impactful work where contributions directly impact patient care and make a meaningful difference.
• The company provides global reach and innovation, fostering collaboration with colleagues worldwide and contributing to global healthcare solutions at the forefront of the diagnostic industry.
• Diasorin fosters a diverse and inclusive culture, valuing unique perspectives and offering a supportive, collaborative environment where everyone can thrive.

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, 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.