Associate, Process Development (Bioprinting)

Aspect-Biosystems; Vancouver; On-site; CAD 64,000 - 72,000; Full time

Job summary

Aspect Biosystems in Vancouver, BC is seeking an Associate, Process Development (Bioprinting CMC) to join our team focused on manufacturing and development of bioprinted tissue therapeutics. You will support therapeutic programs by assisting in production of BTTs, contributing to groundbreaking programs and our mission. The role requires master’s or bachelor’s with experience; familiarity with GMP, GDP; collaborative, fast-paced environment. The position is 100% on-site at our Vancouver office.

Qualifications

• Master's in biomedical engineering, materials science, biochemistry, life sciences, or related field; or a bachelor's with 1–2 years of industry experience.
• Familiarity with biomanufacturing process development, including scale-up and optimization.
• GMP and GDP knowledge with experience in regulated environments.

Responsibilities

• Support GMP-compliant bioprinting production in vitro and in vivo for goals.
• Prepare materials and reagents for BTT processes per GDP.
• Assist in process optimization and scale-up for IND-enabling work.
• Perform routine maintenance of bioprinting equipment.
• Develop and test bioprinting processes to meet project goals.
• Follow SOPs and collaborate with process development teams.
• Ensure cGMP-compliant optimization and scaling strategies.
• Support Bioprinting Design Transfers with R&D, CMC, quality, and regulatory.
• Design and execute studies to qualify new BTTs.
• Collect data and analyze for process improvement.
• Collaborate cross-functionally to refine bioprinting methods.

Skills

Process development exposure

GMP knowledge

GDP knowledge

Collaborative

Effective communication

Go-getter

Education

Master’s in biomedical engineering or related field

Bachelor’s with 1-2 years industry experience

Job description

Associate, Process Development (Bioprinting)

We are seeking an Associate, Process Development (Bioprinting CMC) to join our high-performing team focused on the manufacturing and process development of bioprinted tissue therapeutics (BTT). Reporting to the Senior Manager, Process Development, you will support our therapeutic programs by assisting in the production of various BTTs, directly contributing to our groundbreaking programs and our mission to develop bioprinted tissue therapeutics to transform the lives of people with serious diseases.

Responsibilities

• Supporting in the manufacturing of BTTs in-vitro and in-vivo for Good Manufacturing Practices (GMP) and research and development goals.
• Preparing materials and reagents for BTT processes in compliance with Good Documentation Practices (GDP).
• Helping carry out process optimization and scale up activities to support IND-enabling work for multiple BTT product candidates.
• Performing routine maintenance of bioprinting equipment to support consistent production.
• Assisting in developing and testing bioprinting processes and BTTs to meet project goals.
• Following standard operating procedures (SOPs) and collaborating with process development teams to ensure compliance.
• Ensuring compliance of optimization and scaling strategies with cGMP regulations.
• Working closely with R&D, CMC, quality, and regulatory teams to support Bioprinting Design Transfers (BDT) in compliance with regulatory requirements.
• Designing and executing studies to qualify and characterize new BTTs.
• Performing data collection and analysis to contribute insights for process improvement.
• Collaborating cross functionally to help develop and refine bioprinting methods for different therapeutic applications.
• Creating and following experimental forms, SOPs, batch production records (BPRs), and other documentation as needed.

Qualifications

• Education + Experience: A master’s in biomedical engineering, materials science, biochemistry, life sciences or related field; alternatively, a bachelor’s with 1 - 2 years of industry experience.
• Process Development Exposure: Familiarity with biomanufacturing process development, including scale-up and optimization. Experience in a cGMP setting, especially in cell therapy would be highly beneficial.
• GMP & GDP Knowledge: Basic understanding of Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP), with experience working in regulated environments.
• Collaborative: You thrive in a multi-disciplinary team environment and believethat we can get further, faster by working together.
• Effective Communicator: You are an active listener who can effectivelycommunicate to different audiences in diverse situations.
• Go-Getter: You work with a sense of urgency, are results-driven, and thrive ina fast-paced, interdisciplinary, and entrepreneurial environment. You arewilling to roll up your sleeves and do what it takes to get the job done.

The hiring range for this role is $64,000 - $72,000, 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 equity, 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!

This position is 100% on-site at our Vancouver, BC office.