Staff - Non Union

Job Category
M&P - AAPS

Job Profile
AAPS Salaried - Scientific Eng., Level B

Job Title
Research Engineer, ATMF

Department
Process Development | ATMF | Faculty of Medicine

Compensation Range
$7,158.42 - $10,292.25 CAD Monthly
The Compensation Range is the span between the minimum and maximum base salary for a position. The midpoint of the range is approximately halfway between the minimum and the maximum and represents an employee that possesses full job knowledge, qualifications and experience for the position. In the normal course, employees will be hired, transferred or promoted between the minimum and midpoint of the salary range for a job.

Posting End Date
August 26, 2026

Note: Applications will be accepted until 11:59 PM on the Posting End Date.

Job End Date
September 15, 2027

This position is expected to be filled by promotion/reassignment and is included here to inform you of its vacancy at the University.

Job Summary

The Advanced Therapeutics Manufacturing Facility (ATMF) is a new CFI-funded project and part of Canada's Immuno-Engineering and Biomanufacturing Hub (CIEBH), a UBC-led national research hub that aims to align the critical mass of immune-engineering with biomanufacturing and public health strengths concentrated in BC. This multi-year, multi-phase initiative aims to build a Good Manufacturing Practice (GMP) biomanufacturing core facility to produce advanced therapeutics-such as cells, mRNA vaccines, and ancillary plasmid DNA-essential for early-phase clinical trials, addressing current health challenges, and strengthening Canada's pandemic preparedness

The Research Engineer - Process Development position aims to develop and facilitate the research being conducted at the ATMF. Specifically, the engineer in this position will conduct research, contribute to, coordinate, and lead selected technical workstreams to advance biomanufacturing technologies for various therapeutic products, including plasmids, mRNA/LNP formulations, cell therapy products, and related advanced therapeutics workflows. This role involves designing and optimizing upstream and downstream processes, performing data analysis, developing robust manufacturing protocols, maintaining laboratory equipment, supporting technology transfer to GMP production environments, and collaborating with cross-functional teams. In some instances, the Engineer will also supervise junior staff who are conducting research. The Research Engineer will work with the ATMF Process Development Manager, Project Lead and staff to prepare reports and peer-reviewed publications, present research results at scientific conferences, to funding organizations, and other external stakeholders.

The position is based in a laboratory at the ATMF facility and pilot-scale laboratories. Travel will be required between multiple laboratory sites, including BCCHR, BC Cancer, and UBC Point Grey Campus.

Organizational Status

The Research Engineer will report to the Manager of Process Development, Nucleic Acid Therapies, ATMF.

Works in the Process and Analytical Development lab with other research and technical staff.

Supervises junior technical staff, students or trainees overseeing the team conducting specific experiments in bioprocess, process, and analytical development.

Consults with ATMF managers, staff and other UBC departments, universities, research institutes, vendors, and industry partners in the bioprocess design , technology assessment, equipment selection and workflow implementation.

Work Performed
• Design experimental and analytical investigations related to bioprocess engineering of advanced therapeutic products and/or ancillary materials, including plasmids, mRNA-LNP, cell therapy products, biologics and related advanced therapeutics.
• Execute, and lead optimization of the assigned upstream and downstream process development workflows, which may include pDNA synthesis, IVT, cell culture, transformation, transfection, fermentation, purification, filtration, formulation, and analytical characterization. This includes planning and conducting experiments, operating specialized equipment, analyzing process-performance data, troubleshooting, and independently recommending or implementing changes to process parameters or methods within approved project objectives and in consultation with ATMF Process Development lead, QA/QC and GMP manufacturing personnel as required.
• Conduct experiments, collate data, analyze results and communicate findings in a timely and scientifically rigorous manner.
• Develop or apply mathematical, statistical, and analytical models to support process assessments, including yield, purity, potency, stability, reproducibility, and process performance evaluation.
• Assess and implement bioprocess design alternatives using experimental data, engineering principles, risk assessment, and fit-for-purpose process development strategies.
• Independently perform, verify, and document complex design, and scale-up calculations, and process transfer assessments related to experimental and translational biomanufacturing work; evaluate calculation assumptions and outputs, identify scale-up risks or constraints, and recommend process, equipment or method changes based on the results.
• Develop, optimize, and maintain protocols, standard operating procedures (SOPs), batch record style documents, and other technical documentation for bioprocess workflows.
• Evaluate and integrate new bioprocessing technologies, consumables, analytical tools, and equipment to enhance efficiency, robustness, scalability, and product quality.
• Work with equipment vendors and internal stakeholders to assist with installation, qualification support, calibration, modification, maintenance, troubleshooting and repair of bioprocess and analytical equipment
• Maintain detailed documentation following Good Documentation Practices (GDP) and contribute to GMP-aligned documentation packages in collaboration with QC/QA teams.
• Coordinate technology transfer from process development laboratories to ATMF's GMP laboratories, by assessing transfer readiness, defining technical requirements, compiling transfer documentation, identifying process, equipment, or documentation risks, and recommending adjustments to process parameters, methods, equipment set-up or documentation to ensure alignment with regulatory, quality and operational requirements.
• Participate in hiring, training, mentoring and supervision of junior process and analytical development staff, students, coop interns, or trainees.
• Provide technical assistance and work closely with scientists, operations, engineers, quality teams, vendors, and GMP manufacturing personnel to support bioprocess innovations and translational manufacturing readiness.

Consequence of Error/Judgement
The Research Engineer may have access to confidential data. The quality of work performed will determine the success of ATMF projects and funding. Exercising poor judgment and failing to consult appropriately with research team members and supervisors can adversely affect the viability and validity of ATMF's projects or programs and may compromise UBC and the Department's ability to secure grant-based funding for future ATMF projects.

Supervision Received
The ATMF Process Development Manager will provide overall supervision of this role. However, the Research Engineer may take direction and feedback from senior members of the ATMF. It is important that the Research Engineer be capable of working independently within project objectives.

Supervision Given
The Research Engineer will participate in the hiring, training, and supervision of junior process development staff, students, coop interns, and trainees. The Research Engineer may provide guidance and direction to staff in carrying out experiments, protocol development, equipment evaluation, data analysis, process optimization, documentation and troubleshooting.

Minimum Qualifications
Undergraduate degree in Engineering or Applied Science. Minimum of three years of related experience, or the equivalent combination of education and experience.

- Willingness to respect diverse perspectives, including perspectives in conflict with one's own

- Demonstrates a commitment to enhancing one's own awareness, knowledge, and skills related to equity, diversity, and inclusion

Preferred Qualifications
• Master's degree in Bioprocess/Chemical Engineering, Biochemistry, Biotechnology, Pharmaceutical Sciences or a related field.
• Experience in hands-on experience with bioprocessing techniques and equipment, including bioreactors, depth filtration, chromatography and tangential flow filtration systems, and formulation.
• Strong analytical skills and experience with process design, experimental design, process characterization, troubleshooting, optimization and data interpretation.
• Experience supporting scale up, process transfer, or translation of research-stage workflows toward GMP-ready or clinical-grade production environment is an asset.
• Knowledge of automation, process control, high-throughput screening, data analysis, workflows, or digital tools for process & analytical development is an asset.
• Ability to prepare clear, concise, and accurate research reports, technical reports, protocols, and presentations.
• Experience in working with LIMS, electronic lab notebooks, and data management systems.
• Familiarity with regulatory frameworks such as Health Canada, FDA, and EMA guidelines for cell and gene therapies is an asset.
• Ability to work a flexible schedule, including occasional weekends, evenings, and early mornings, as required.
• Ability to work both independently and collaboratively in a team environment.
• Demonstrated ability to work in a fast-paced, collaborative research environment.
• Strong commitment to continuous learning, adaptability, scientific rigour, and operational excellence.