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Added 4 mins ago
AC
Manager, Tax / Directeur(trice), Fiscalité
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- Full-time
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SP
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DiaSorin

ASSOCIATE SCIENTIST I - AGS

Toronto, ON, M5G 1Y8, Canada

Apply About employer

Applications open in a new tab.

Job details

Apply by: Nov 6, 2026
Posting language: English
Posted: Nov 2, 2026

Original job description

Obsessed by Science. Entrepreneurial by Nature. United by Purpose.

Diasorin is a global leader in immunodiagnostic and molecular diagnostic solutions, advancing science to improve patient outcomes worldwide. For more than 50 years, we have combined scientific rigor with an entrepreneurial mindset, operating with a strong commitment to innovation, accountability, and results to deliver trusted diagnostic solutions.

As the Diagnostics Specialist, Diasorin continuously invests in research, technology, and people. Guided by our values of operational excellence, customer focus, and teamwork, we empower teams to think boldly, act decisively, and transform ideas into meaningful impact across one of the industry’s broadest specialty diagnostic portfolios.

When you join Diasorin, you are not just filling a role. You are helping build what comes next.

Why Join Diasorin

Build What Matters
Take ownership, challenge the status quo, and contribute directly to solutions that improve patient care worldwide.
Innovate with Agility at a Global Scale
Work in an entrepreneurial environment that enables speed, collaboration, and global impact.
Grow in a People-Centered Culture
Thrive in a culture that values accountability, inclusion, and continuous development.

Job Scope

The Associate Scientist I - AGS is responsible for participating 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.

Job Responsibilities

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, 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 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

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

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 committed to building a workplace where people feel empowered to contribute ideas, take ownership, and grow their careers. We believe diverse perspectives strengthen innovation and help us deliver meaningful impact for patients and customers worldwide.

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.

This posting and recruitment process are subject to applicable local laws and regulations in the country where the position is located. Additional employment disclosures, candidate rights, and employment conditions may apply based on local jurisdiction.

Individuals hired will be required to verify identity and eligibility to work and may be subject to a background check and drug screening where permitted by law. Diasorin is committed to providing reasonable accommodations for qualified individuals with disabilities during the application process. If assistance is required, please contact hr@diasorin.com.

Recruitment Fraud Notice

Diasorin never requests payment, financial information, or personal banking details from candidates at any stage of the recruitment process. Official communications from Diasorin recruiters will only come from a verified @diasorin.com email address. If you have questions about the legitimacy of a recruitment communication, please contact hr@diasorin.com for verification.

Unauthorized third-party recruiting agencies may not submit candidates for this position without prior written authorization from the Diasorin Human Resources Department.

Apply About employer

More about this job

Responsibilities

Conduct and interpret laboratory experiments for the development of sequencing, fragment analysis, and other molecular assays, while generating, analyzing, and documenting experimental data. Contribute to protocols, reports, intellectual property development, design control compliance, and cross-functional coordination with regulatory, clinical, assay R&D, and quality teams.

Requirements

Requires a two-year technical associate degree in a relevant scientific field plus at least two years of molecular biology or biotechnology laboratory experience; a bachelor's degree in a related discipline is preferred. Requires at least one year of experience with molecular and biochemical procedures, including PCR, data analysis, specimen processing, and documentation; sequencing methods, CL2 procedures, ISO 13485, FDA regulations, and medical device experience are preferred.

Skills

Molecular Biology
PCR
Sanger Sequencing
Next-Generation Sequencing
Digital PCR
Real-Time PCR
Data Analysis
Experimental Documentation
Specimen Handling
Laboratory Procedures
Technical Writing
Design Controls
ISO 13485
FDA Regulations
Troubleshooting
Microsoft Office

Visa sponsorship

Not detected in the job text

Keywords

Research And Development
Molecular Assays
Molecular Biology
Biotechnology
PCR
Real-Time PCR
Digital PCR
Sanger Sequencing
Next-Generation Sequencing
Fragment Analysis
Biochemistry
Experimental Design
Data Analysis
Specimen Handling
Experimental Documentation
Feasibility Studies
Verification
Validation
Quality System Requirements
Design Controls
FDA Regulations
ISO 13485:2016
Containment Level 2
Intellectual Property
Technical Writing
Troubleshooting
Laboratory Organization
Regulatory Affairs
Clinical Affairs
Quality Assurance

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