IVD Process & Product Transfer Engineer — Stock Options

spearbio

Saint-Augustin-de-Woburn

On-site

CAD 70,000 - 110,000

Full time

14 days+

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Job summary

Spear Bio is seeking an Associate Engineer/Scientist, Process & Product Transfer to lead new product introduction (NPI) design transfer activities and translate assay designs into scalable manufacturing instructions. The role emphasizes cGMP-compliant documentation, cross-functional teamwork, and hands-on process transfer from development to production.

The ideal candidate will have hands-on experience in immunoassay development or manufacturing within the diagnostics industry, with strong

Qualifications

Experience in product or technology transfer within the diagnostics industry under cGMP requirements to support product launches.
Experience with IVD or RUO diagnostic assay kit manufacturing.
Experience with process validation, statistical analysis, and continuous improvement methodologies.
Demonstrated project management skills.
Familiarity with design controls during the product development process.
Familiarity with Good Documentation Practices, cGMP requirements, FDA and/or ISO quality standards for medical device and IVD products.
Familiarity with CLSI guidelines is a plus.
High attention to detail to ensure accuracy and consistency in documentation and batch record execution.
Strong analytical and problem-solving skills to address and resolve technical issues.
Excellent communication skills to effectively collaborate with cross-functional teams.
Proficiency in Excel for creating manufacturing records and data analysis templates.
Experience leveraging AI tools to support process automation is a plus, with appropriate human-in-the-loop oversight.

Responsibilities

Lead new product introduction (NPI) design transfer activities and ensure all required deliverables are completed in alignment with Product Development Process requirements.
Develop specifications and acceptance criteria for raw materials or in-process materials to ensure product quality.
Translate assay designs into manufacturing work instructions and in-process test instructions that can be easily understood by manufacturing operators.
Build assay reagents at scale during feasibility and design verification phases while ensuring batch records are completed in accordance with cGMP requirements.
Plan and execute process verification experiments to demonstrate the robustness and reproducibility of assays being transferred.
Ensure material transactions are completed in a timely manner to maintain accurate inventory control.
Drive lean manufacturing, process improvement, and supply chain initiatives to improve cost of goods, efficiency, yield, and quality.
Lead investigations during design transfer and provide resolutions for product and process issues.
Develop electronic records for manufacturing work instructions and create data analysis templates to improve efficiency and reduce errors.
Maintain detailed records of manufactured materials during the transfer process and complete batch records following cGMP requirements.
Review executed batch records and work with QA to address any quality issues prior to release (deviation, NCMR, CAPA, change control).
Ensure all process documentation is accurate, complete, and compliant with regulatory standards (e.g., FDA, ISO).
Support regulatory submissions, audits, and inspections as required.