Associate Process Engineer (12 month contract)

We're looking for an enthusiastic Associate Process Engineer to join our dynamic and dedicated Process Development team. Reporting to the Head of Process Development, you will support the development of an aseptic manufacturing workflow for our bioprinted tissue therapeutics. You’ll be joining a company committed to developing regenerative medicines that deliver life-changing, functional cures for patients living with serious diseases. . Responsibilities Assisting in the design, execution, and characterization of fluidic systems, bioreactor scaling strategies, and automated cell processing workflows (wash, concentrate, harvest) to support process robustness. Collaborating with Process Development, Bioengineering, Engineering, and Manufacturing team members to support technical integration of the cell therapy process into the final device platform, focusing on closed-system design and single-use technologies. Participating in process risk assessments (e.g., FMEA, PHA) for both the cell manufacturing process and its interaction with the medical device component. Utilizing mathematical models and Design of Experiments (DOE) methodologies under senior guidance to assist in defining critical process parameters (CPPs) and critical quality attributes (CQAs). Supporting technology transfer to Manufacturing, including assisting with process qualification and early phase clinical manufacturing as needed. Contributing to technical troubleshooting and assisting with out-of-specification investigation and root cause analysis during manufacturing deviations or process improvements. Supporting the execution of validation strategies for sterilization, biocompatibility, and extractables/leachables (E&L), and helping compile technical data for regulatory filings (CTA/IND). Identifying process improvement opportunities in current cell therapy manufacturing to help optimize yield, purity, and scalability. Continuously building your technical expertise while contributing to a culture of rigor and data-driven decision-making. Qualifications Education + Experience: M.S. or BSc. in Chemical Engineering, Bioengineering, Biomedical Engineering, or a related life science field with 1-2+ years of relevant industry experience, in cell therapy, bioprocess development, or biologics manufacturing. Process Development & Characterization Experience: Hands-on background in the development, characterization, and optimization of biomanufacturing processes is required, preferably within cell therapy. Bioreactors: Experience with bioreactor systems and scaling strategies is desirable. GMP & GDP Knowledge: Knowledge of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP). Familiarity with regulatory requirements for cell therapy products (e.g., providing technical content for CTA/IND filings). Analytical and Communication Skills: Analytical, problem-solving, and data-driven decision-making skills. Excellent written and verbal communication skills, including the ability to present complex data and mentor junior team members. The hiring range for this role is $64,000 - $72,000 CAD annually. Our ranges are based on market data. Offered salaries will be based on a combination of factors including, but not limited to, job-related knowledge, skills, education, and experience. For candidates who exceed role requirements, we are open to exploring above-range offers. Note that base salary is just one part of the overall compensation at Aspect. Members of the Aspect team also receive a comprehensive benefits package, and support for continuous learning and career progression. Who We Are 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! Curious about our current perks and benefits? Learn more here. 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, 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. 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!

The Associate Process Engineer will support the development of aseptic manufacturing workflows for bioprinted tissue therapeutics, including fluidic system design and bioreactor scaling. They will also collaborate with cross-functional teams to integrate processes into device platforms and support technology transfer to manufacturing.

Candidates must hold a BSc or MSc in Chemical, Bio, or Biomedical Engineering with 1-2+ years of relevant industry experience in cell therapy or bioprocessing. Proficiency in GMP/GDP and hands-on experience with biomanufacturing process characterization are required.

• Comprehensive benefits package • Continuous learning support • Career progression support

Identified from the job description. Confirm important requirements above.

• Process development
• Biomanufacturing
• Cell therapy
• Bioreactor systems
• GMP
• GDP
• Fluidic systems
• Design of experiments
• Technical troubleshooting
• Root cause analysis
• Regulatory filings
• Data-driven decision-making
• Bioprocess development
• Scaling strategies
• Aseptic manufacturing
• Endocrine Diseases And Disorders
• Good Documentation Practices
• Continuous Development
• Full Stack Development
• Workflow Management
• Curiosity
• Medical Devices
• Data-Driven Decision Making
• Artificial Intelligence
• Automation
• Biomedical Engineering
• Biotechnology
• Biocompatibility
• Biological Engineering
• Biology
• Biopharmaceuticals
• Bioprocess
• Good Manufacturing Practices
• Cell Therapy
• Chemical Engineering
• Communication
• Design of Experiments (DOE)
• Diabetes Mellitus
• Endocrinology
• Process Engineering
• Sterilization
• Failure Mode And Effects Analysis
• Scalability
• Problem Solving
• Manufacturing Processes
• Mathematical Modeling
• Metabolic Diseases And Disorders
• Process Development
• Regenerative Medicine
• Risk Analysis

• Engineering
• Science & Research
• Healthcare
• Manufacturing
• Process Engineer
• Process Engineer (General)
• Industrial and Production Engineers
• Chemical Engineers

Minimum education

Bachelor’s degree

Minimum experience

2+ years

Posting language

English

Working hours

40 hours per week