Scientist - I

VitalBio•Oakville, ON

15h•CA$65,000 - CA$85,000

About The Position

This role is for a detail-oriented scientist with a strong foundation in biological sciences and a keen interest in immunoassay development. The ideal candidate is highly motivated, eager to learn, and comfortable working in a fast-paced, inter-disciplinary environment. This position requires hands-on lab experience from academic or industry settings and offers the opportunity to contribute to the development of high-quality diagnostic products.

Requirements

Bachelor’s or Master’s degree in Life Sciences, Biochemistry, Bioengineering, or related field.
0-2 years of laboratory experience in academic or industry settings (internships, co-ops or research projects).
Foundational understanding of immunoassay principles (eg: ELISA, lateral flow assays) and laboratory best practices.
Basic hands-on experience with common lab techniques and data analysis tools.
Strong organizational, written and verbal communication skills.
A collaborative mindset with a willingness to take on new challenges and learn from others.
Commitment to lab safety, quality standards and continuous improvement.

Nice To Haves

Experience with nanoparticles, microfluidics or automated laboratory systems.
Prior exposure to technology transfer or manufacturing environments.
Experience writing SOPs and lab documentation.
Familiarity working in a startup or regulated diagnostics environment.
Appreciation for puns and a positive, team-oriented attitude!

Responsibilities

Support the design and execution of experiments for immunoassay development, integration and validation.
Accurately document experimental results and compile data for review and presentation at internal meetings.
Assist with troubleshooting and continuous process improvement efforts as needed.
Operate and maintain laboratory instrumentation such as plate readers, liquid handlers and other relevant tools.
Contribute to the preparation of technical documentation and support technology transfer.
Follow standard operating procedures (SOPs) and quality guidelines to ensure compliance with regulatory standards (eg: cGMP, ISO 13485).
Assist with lab organization, including inventory management and routine maintenance of supplies and equipment.
Collaborate with cross-functional teams (product development, engineering, quality, and manufacturing) to support project timelines and deliverables.
Understand and adhere to company guidelines on code of conduct and lab safety practices to ensure an organized and compliant laboratory environment.