We are seeking a Scientist, Process Development (Bioprinting CMC) to join our high-performing team focused on the manufacturing and process development of bioprinted tissue therapeutics (BTT). In this role, you will support Aspect’s therapeutic programs by driving the production of various BTTs, directly contributing to Aspect’s groundbreaking programs and our mission development of bioprinted tissue therapeutics to transform the lives of people with serious diseases. The majority of your time will be spent in the lab, driving hands-on experimentation and analysis to refine and validate processes. Your contributions will be critical in advancing healthcare, driving the development of bioprinted tissue therapeutics that have the potential to revolutionize the treatment of diseases previously deemed incurable.

QUALIFICATIONS

• Education + Experience: A master’s in biomedical engineering, materials science, biochemistry, life sciences or related field, accompanied by a minimum of 5 years of industry experience; alternatively, a bachelor’s with at least 7 years of industry experience.
• Analytical Techniques and Proficiency: Skilled in mechanical testing, microscopy, and other assays with expertise in statistical process control methodologies.
• Design of Experiments (DOE): Experienced in utilizing DOE methodologies for process optimization and analysis.
• Preferred familiarity: Familiarity with 3D printing techniques, cell culture, and biomaterials is strongly preferred.
• Process Development Experience: Strong background in the development, scale-up, and optimization of biomanufacturing processes in a cGMP setting ideally in the cell therapy space.
• GMP & GDP Knowledge: Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).

WHO WE ARE

Aspect Biosystems is a Canadian biotechnology company creating bioprinted tissue therapeutics to transform how we treat disease. Our bold team of innovators and entrepreneurs have joined us from all over the globe to create a new class of regenerative medicine and work towards a future where our bioprinted tissues are used to save lives and make people healthier. We are endlessly curious and wildly passionate about what we do. Every person on our team is a key contributor to our success and is eager to roll up their sleeves to make a difference in the ever-changing world of biotech. 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. Different people, thinking differently, unified in creating a world that is better for us all. We are committed to creating an inclusive environment for everyone on our team. 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, colour, religion, marital status, age, national origin, ancestry, physical or mental disability, medical condition, pregnancy, genetic information, gender, sexual orientation, gender identity or expression, veteran status, or any other status protected under federal, provincial, or local law.
If you’re interested in joining our team but don’t see a job posting that matches your experience or background, we encourage you to submit a general application to be considered for future opportunities

• Drive the manufacturing and development of BTTs in both in-vitro and in-vivo environments to support Aspect’s Good Manufacturing Practices (GMP) and research and development goals.
• Design and execute experiments to optimize bioprinting processes for production of BTTs.
• Collaborate extensively with Aspect’s Technical Operations, Research and Development, and Engineering teams to innovate, optimize, and translate laboratory -scale bioprinting processed to scalable manufacturing operations.
• Establish and perform rigorous testing and validation protocols for bioprinted constructs to ensure they meet predefined specifications for structure, function, and biological activity.
• Develop and characterize process parameters to ensure reproducibility, scalability, and quality of bioprinted constructs.
• Provide technical support for troubleshooting and root cause analysis during manufacturing deviations or process improvements.
• Ensure the preparation of materials and reagents for BTT processes adheres to Good Documentation Practices (GDP).
• Lead the development, characterization, and validation of bioprinting to meet project-specific and company-wide milestones.
• Support the maintenance and operational efficiency of bioprinting equipment, ensuring continuous and effective production workflows.
• Ensure that optimization and scaling strategies for BTT production align with current Good Manufacturing Practices (cGMP) regulations.
• Create, review, and maintain experimental forms, SOPs, Batch Production Records (BPRs), experimental report writing, and other essential documentation to support CMC and R&D activities.
• Ensure all processes and procedures are meticulously documented and comply with relevant regulatory and quality standards.
• Foster strong partnerships with internal teams and external experts to support the continuous improvement of bioprinting technologies and therapeutic applications.
• Act as a subject matter expert in bioprinting process development, providing insights and guidance to drive innovation and operational excellence.
• Present findings and progress reports to internal teams and external collaborators.