Scientist I- IA

Vital Bio • Oakville, ON

41d • CA$65,000 - CA$85,000 • Onsite

About The Position

This role is for a detail-oriented scientist with a strong foundation in biological or chemical 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 innovative, impactful diagnostic products.

Requirements

• Bachelor’s or Master’s degree in Life Sciences, Biochemistry, Bioengineering, or related field.
• 2+ years of laboratory experience in academic or industry settings
• 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, automated laboratory systems, protein conjugation or immobilization chemistry, statistical analyses.
• Prior exposure to technology transfer, general assay development, or obtaining regulatory approval.
• Experience writing SOPs and lab documentation, experience with eQMS systems.
• Familiarity working in a startup environment, and a demonstrated ability to creatively problem solve
• Appreciation for puns and a positive, team-oriented attitude!

Responsibilities

• Design and execute 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 (clinical, regulatory, 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.

Benefits

• Compensation will be determined based on the individual’s demonstrated experience, education, training, relevant certifications or licensure, and other applicable business and organizational factors.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: Associate degree