Immunoassay Scientist II: Diagnostics Innovation

Socket.dev

Oakville

On-site

CAD 80,000 - 95,000

Full time

14 days+

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Job summary

Vital Bio is seeking a detail-oriented scientist to lead immunoassay development in a fast-paced, interdisciplinary environment. You will design, execute, and analyze experiments, document results, troubleshoot assays, and optimize instrumentation such as plate readers and liquid handlers, to support regulatory-ready workflows for cGMP/ISO 13485 compliance.

This onsite role in Oakville, Canada offers the opportunity to grow technical ownership while contributing to innovative diagnostic products

Qualifications

Bachelor’s or Master’s degree in Life Sciences, Biochemistry, Bioengineering, or a related field.
4+ years of laboratory experience in academic or industry settings.
Strong understanding of immunoassay principles such as ELISA and lateral flow assays.
Hands-on experience with common lab techniques and data analysis tools.
Experience interpreting experimental data and contributing to assay troubleshooting or optimization.
Strong organizational, written, and verbal communication skills.
A collaborative mindset with the ability to work independently and take ownership of assigned work.
Commitment to lab safety, quality standards, and continuous improvement.

Responsibilities

Design, execute, and independently analyze experiments for immunoassay development, integration, and validation.
Document experimental results clearly and present data at internal meetings and project reviews.
Troubleshoot assay performance issues and contribute to continuous process improvement efforts.
Operate, maintain, and help optimize laboratory instrumentation such as plate readers, liquid handlers, and other relevant tools.
Contribute to technical documentation, assay workflows, and technology transfer activities.
Follow standard operating procedures and quality guidelines to support compliance with regulatory standards such as cGMP and ISO 13485.
Support lab organization, including inventory management, equipment maintenance, and supply tracking.
Collaborate closely with clinical, regulatory, engineering, quality, and manufacturing teams to support project timelines and deliverables.
Help drive experimental planning, data interpretation, and decision-making for assay development programs.
Adhere to company guidelines on code of conduct and lab safety practices to maintain an organized and compliant laboratory environment.