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Aspect Biosystems Verified
Biotechnology

Associate Process Engineer (12 month contract)

VancouverOnsiteContractEntry-level (exp-based)CA$64,000–CA$72,000 /yrPosted 2 months ago

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Required skills

  • aseptic manufacturing
  • bioprinted tissue therapeutics
  • regenerative medicines
  • cell therapy
  • bioprocess development
  • biologics manufacturing
  • fluidic systems
  • bioreactor scaling
  • automated cell processing
  • closed-system design

Nice to have

  • bioreactor systems
  • scaling strategies
  • GMP
  • GDP
  • regulatory requirements

Role summary

Aspect Biosystems is seeking an Associate Process Engineer for a 12-month contract to support the development of an aseptic manufacturing workflow for bioprinted tissue therapeutics. The role involves assisting in the design and execution of fluidic systems, bioreactor scaling, and automated cell processing, with a focus on closed-system design and single-use technologies. Responsibilities include participating in process risk assessments, utilizing DOE methodologies, supporting technology transfer, troubleshooting, and contributing to validation strategies for sterilization, biocompatibility, and E&L. The position requires an M.S. or BSc. in a relevant engineering or life science field with 1-2+ years of industry experience in cell therapy or bioprocess development. Familiarity with GMP, GDP, and regulatory requirements for cell therapy products is preferred. The role offers a salary range of $64,000 - $72,000 CAD annually.

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.

    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!

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