We are seeking a Quality Assurance Specialist to strengthen and oversee our quality assurance development. You will pioneer and execute quality assurance activities associated with clinical Positive Manufacturing Practices (GMP) of our bioprinted cell therapies. With a passion for optimization, you will also drive continuous improvement of our manufacturing and quality systems by developing, applying, revising, and maintaining quality metrics.

Support in development of internal QA processes and procedures and implementation of the company’s Quality Management System (QMS). Maintain and provide document control support. Assist in development of training content for QA processes, maintain training and certification requirements for the position.

Provide QA expertise on change management, and support implementation of documents, design, process, and material related changes. Collaborate closely with R&D; teams from the early development phases to embed quality standards directly into product designs, technical documentation, and underlying engineering processes Be the quality assurance and documentation expert and support cross-functional groups on: Creating, reviewing, approving, and implementing SOPs, Policies, forms, and other controlled documents Reviewing data for completeness Completing root cause analysis/ investigations and implementing appropriate corrective and preventive actions. Collaborate routinely with the CMC and QC teams during processing, bioprinting and testing, ensuring buy-in and ownership of our quality program.

Assist in the development of critical raw material specifications and review and approve incoming raw materials. Support in the development and implementation of critical CMC equipment qualification. Assist in Risk Management by conducting risk assessments on core raw materials.

Education & Experience: You hold a Bachelor's degree or Master’s degree inBiology,



Biotechnology or another relevant discipline and 5-7+ years of hands‑on experience developing, or administrating GMP quality programs in biotech, medical device, or pharmaceutical environments.

Regulatory Expertise: Demonstrated knowledge and application of industrial regulations including those of FDA, EMEA, and other authorities related to Biologics and/or Pharmaceuticals.

Experience with medical device regulations is a plus. Our ranges are based on market data. Members of the Aspect team also receive equity, a comprehensive benefits package, and support for continuous learning and career progression.

Aspect

Biosystems is a biotechnology company pioneering the development of a novel category of regenerative medicine designed to restore or supplement biological function and deliver curative therapies for some of the most elusive diseases. Aspect is developing these bioengineered cellular medicines by applying its full‑stack tissue therapeutic platform, which integrates proprietary AI‑powered bioprinting technology, therapeutic cells, hypoimmune cell engineering, and advanced biomaterials. Aspect is advancing its therapeutic pipeline across multiple endocrine and metabolic diseases, including diabetes and rare endocrine disorders.

If you are committed to making a real impact and accelerating the development of life‑changing therapies, we want to hear from you!

At Aspect

Biosystems, our strength has always been in our diversity. All aspects of employment — including the decision to hire, promote, discipline, or terminate — are based on merit, competence, performance, and business needs. We do not discriminate on the basis of race, color, religion, citizenship status, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, political affiliation, or any other status protected under federal, state, provincial, or local law.

📌 Quality Technician (Medical) (Vancouver)
🏢 Aspect Biosystems
📍 Vancouver