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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, and 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

• Participate in day-to-day R&D activities, including design, execution, and interpretation of scientific experiments.
• Design and develop assays based on Luminex's technology platform and chemistries.
• Handle scientific experiments independently with minimal supervision.
• Perform hands-on laboratory work, including planning and designing experiments.
• Generate, record, and analyze experimental data.
• Maintain 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 work closely with other functional groups (Quality Affairs, Regulatory Affairs, Clinical Affairs, Design Transfer, Manufacturing, Quality Control) regarding priorities and timetables.
• 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 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.
• 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 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).

Skills

• Molecular biology
• Biotechnology
• PCR
• Data analysis
• Specimen handling and processing
• Experimental documentation
• ISO 13485:2016
• FDA regulations
• Medical device industry
• Microsoft Word
• Microsoft Excel
• Microsoft PowerPoint
• Time management
• Prioritization
• Independent work
• Teamwork
• Design Control
• Mathematics
• Statistics
• Technical writing

Location

• United States
• Canada

Work Type

• Full-time

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)
• 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

Benefits

• Competitive salary and benefits package

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, 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."
• 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.
• 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.
• 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.
• 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!

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.