Associate Process Engineer, Cell Therapy

Job type:; Vancouver; On-site; CAD 64,000 - 72,000; Full time

Benefits offered by this job

Comprehensive benefits package

Job summary

Aspect Biosystems is seeking an Associate Process Engineer to support aseptic manufacturing workflows for innovative bioprinted tissue therapeutics. You will work under the Head of Process Development to design and optimize closed-system, single-use processes, and contribute to technology transfer to Manufacturing.

The role requires 1-2+ years in cell therapy or biologics manufacturing, with strong analytical and communication skills, and familiarity with GMP/GDP and regulatory filings.

Qualifications

• Hands-on background in development, characterization, and optimization of biomanufacturing processes.
• Experience with cell therapy or biologics manufacturing is preferred.
• Familiarity with regulatory content for CTA/IND filings is a plus.

Responsibilities

• Assist in design, execution, and characterization of fluidic systems and bioreactor scaling to support process robustness.
• Collaborate with Process Development, Bioengineering, Engineering and Manufacturing teams for integration into the final device platform.
• Participate in process risk assessments (FMEA, PHA) for cell manufacturing and device interaction.
• Apply DOE methodologies to define CPPs and CQAs under senior guidance.

Skills

Process development

Bioreactor scaling

GMP & GDP knowledge

Analytical skills

Education

MS or BSc in Chemical/Bio/Biomedical Engineering or related life science field

Job description

Aspect Biosystems is seeking an Associate Process Engineer to support aseptic manufacturing workflows for innovative bioprinted tissue therapeutics. You will work under the Head of Process Development to design and optimize closed-system, single-use processes, and contribute to technology transfer to Manufacturing.

The role requires 1-2+ years in cell therapy or biologics manufacturing, with strong analytical and communication skills, and familiarity with GMP/GDP and regulatory filings.