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Added 12 days ago
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…scalable infrastructure for AI agents, as well as optimize data processing and develop automated systems for model…
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Aspect Biosystems

Scientist, Analytical Development

Vancouver, BC, Canada

Pay: The hiring range for this role is $90,000 - $96,300, annually.
Posting language: English
Posted: Sep 14, 2026

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Original job description

We're looking for a Scientist, Analytical Development to join our technical operations team. In this role, you'll be instrumental in developing, optimizing, and qualifying analytical methods that support our cutting-edge bioprinted tissue therapeutics. Reporting to our Head, Quality Control and Analytical Development, you'll play a crucial part in ensuring the quality and characterization of our innovative products as we advance toward clinical development.

Responsibilities

Design, execute, and optimize a variety of analytical methods (e.g. cell-based assays, bioanalytical and flow cytometry methods) for the characterization, release, and stability testing of raw materials, in-process samples, and final drug products.
Participate in and execute experiments for the qualification and validation of analytical methods in accordance with phase-appropriate regulatory guidelines (e.g., ICH, FDA, Health Canada, EMA).
Perform routine analytical testing as needed to support process development, product characterization, and early-stage stability studies.
Accurately record, analyze, interpret, and present experimental data. Author and review technical reports, study protocols, and standard operating procedures (SOPs) in compliance with GxP principles.
Identify and troubleshoot analytical method issues, propose solutions, and implement corrective actions.
Work cross functionally with Process Development, Quality Control, Research & Development, and Manufacturing to support product development milestones and resolve analytical challenges.
Perform routine maintenance and calibration of analytical instruments and ensure proper functioning.
Adhere to and contribute to the development of robust analytical quality systems, ensuring data integrity, traceability, and compliance with internal and external regulations.

Qualifications & Experience

Education & Experience: Bachelor's or Master's degree in a relevant scientific discipline with 3-5 years of relevant experience in analytical development within the biotechnology or pharmaceutical industry with hands-on experience in cell therapy, gene therapy, or combination products.
Analytical Expertise: Proven hands-on experience with a range of analytical techniques, such as flow cytometry, ELISA, and/or cell-based assays.
GxP Knowledge: Familiarity with GxP principles (GLP, GMP) and an understanding of regulatory expectations for analytical method development, qualification, and validation for biologics or advanced therapies.
Problem-Solver: You have a keen eye for detail and a methodical approach to troubleshooting analytical challenges.
Innovation Mindset: You're eager to learn new techniques and contribute to the continuous improvement of analytical processes.

The hiring range for this role is $90,000 - $96,300, annually. Our pay scales are based on market data to ensure that compensation is competitive and fair. 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. Base salary is just one part of the overall compensation at Aspect, team members 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!

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More about this job

Responsibilities

The scientist will develop, optimize, and qualify analytical methods to support the characterization and release of bioprinted tissue therapeutics. They will also author technical reports, maintain analytical instruments, and collaborate cross-functionally to ensure compliance with GxP principles.

Requirements

Candidates must hold a Bachelor's or Master's degree in a scientific discipline with 3-5 years of experience in analytical development within the biotech or pharmaceutical industry. Proficiency in analytical techniques like flow cytometry or ELISA and familiarity with GxP regulatory guidelines are required.

Skills

Analytical development
Flow cytometry
ELISA
Cell-based assays
Bioanalytical methods
Method validation
Method qualification
GxP
GLP
GMP
Data analysis
Technical writing
Troubleshooting
SOP development
Instrument calibration
Biotechnology

Benefits

Equity
Continuous learning support
Career progression support

Visa sponsorship

Not detected in the job text

Keywords

Analytical Development
Biotechnology
Bioprinting
Tissue Therapeutics
Cell Therapy
Gene Therapy
Flow Cytometry
ELISA
GxP
GLP
GMP
ICH
FDA
EMA
Method Validation
Method Qualification
Stability Testing
Data Integrity
Technical Operations
Regenerative Medicine
Bioengineered Cellular Medicines
AI-powered bioprinting
Hypoimmune cell engineering
Biomaterials
SOP
Quality Control
Regulatory Guidelines
Process Development
Drug Products
Calibration

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