Senior Process Engineer (12 Month Contract)

Aspect-Biosystems; Vancouver; On-site; CAD 173,000 - 183,000; Full time

Benefits offered by this job

Benefits package

Learning & career progression support

Job summary

Aspect Biosystems is seeking a Senior Process Engineer to lead the development of aseptic bioprocess workflows within the Process Development team. You will work on scalable bioreactor strategies, closed-system design, and automated cell processing, reporting to the Head of Process Development.

The role emphasizes process characterization, DOE-driven optimization, and cross-functional collaboration with Manufacturing, Bioengineering, and Quality to ensure robust technology transfer and

Qualifications

• MS or PhD in Chemical Engineering, Bioengineering, Biomedical Engineering, or related life science with 6–8+ years of industry experience.
• Strong background in development, characterization, and optimization of biomanufacturing processes, preferably in cell therapy.
• Experience with GMP/GDP and regulatory content for CTA/IND filings, and design control frameworks.

Responsibilities

• Lead conceptualization, design, implementation and characterization of complex fluidic systems and bioreactor scaling strategies.
• Coordinate technology transfer to Manufacturing, including process qualification and validation activities (sterilization, E/L).
• Develop mathematical models and apply DOE to define CPPs and CQAs.
• Support regulatory filings and risk assessments (FMEA/PHA) for cell therapy and device interfaces.
• Provide technical mentorship and foster data-driven decision-making within the team.

Skills

DOE (Design of Experiments)

Analytical thinking

Data-driven decision making

Problem solving

Mentoring

Education

MS or PhD in Chemical Engineering / Bioengineering / Biomedical Engineering

Tools

DOE software

Job description

Senior Process Engineer (12 Month Contract)

We're looking for a highly motivated Senior Process Engineer to take on an important role in our dynamic and dedicated Process Development team. Reporting to the Head of Process Development, you will work on developing 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

• Leading the conceptualization, design, implementation and characterization of complex fluidic systems, bioreactor scaling strategies, and automated cell processing workflows (wash, concentrate, harvest) to reduce process risk and improve robustness.
• Working with Process Development, Bioengineering, Engineering and Manufacturing to ensure seamless technical integration of the cell therapy process into the final device platform, focusing on closed-system design and single-use technologies.
• Leading process risk assessments (e.g., FMEA, PHA) for both the cell manufacturing process and its interaction with the medical device component.
• Developing mathematical models and implementing approaches such as DOE (Design of Experiments) to help define critical process parameters (CPPs) and critical quality attributes (CQAs).
• Supporting technology transfer to Manufacturing including support for process qualification as well as assisting in early phase clinical manufacturing as needed.
• Providing technical support for troubleshooting and participating in out-of specification and root cause analysis during manufacturing deviations or process improvements.
• Working with our Quality team to define the validation strategies for sterilization, biocompatibility, and extractables/leachables (E&L) as well as providing the technical backbone for regulatory filings (CTA/IND).
• Identifying gaps in current cell therapy manufacturing and developing patentable technologies to improve yield, purity, and scalability.
• While an individual contributor role, you will mentor others and foster a culture of technical excellence and rigorous data-driven decision-making.

Qualifications

• Education + Experience: M.S. or Ph.D. in Chemical Engineering, Bioengineering, Biomedical Engineering, or a related life science field with 6-8+ years of relevant industry experience, in cell therapy, bioprocess development, or biologics manufacturing.
• Process Development & Characterization Experience: Strong hands-on background in the development, characterization, and optimization of biomanufacturing processes is required, preferably within cell therapy.
• Process Engineering and Characterization: Expertise in the design, implementation, and characterization of complex fluidic systems, including automated cell processing workflows (e.g., wash, concentrate, harvest). Proven ability to develop mathematical models and apply statistical methods (such as Design of Experiments, or DOE) for process characterization and defining Critical Process Parameters (CPPs) and Critical Quality Attributes (CQAs).
• Bioreactors: Experience with bioreactor systems and scaling strategies is desirable.
• GMP & GDP Knowledge: Thorough 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).
• Medical Device Knowledge: Direct experience operating within a Design Control framework (e.g., FDA 21 CFR Part 820) for medical devices, specifically related to process inputs/outputs and risk management is desirable.
• Technology Transfer: Experience supporting technology transfer from Process Development to Manufacturing, including process qualification and validation activities (e.g., sterilization, E&L).
• Analytical and Communication Skills: Strong 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 $124,737 - $131,689, 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.