Artron Laboratories Inc is a technology-based manufacturer specialized in the development and large-scale production of lateral flow rapid test kits. Artron established itself in the progression of in vitro diagnostic lateral flow tests that have revolutionized the market for disease diagnosis and analyte detection. At Artron, we are committed to going above and beyond to meet the specific challenges faced by the rapid diagnostic industry participants. Our mission is to overcome industry challenges and provide simple and affordable IVD products that meet customer's highest expectations.
Our BC head office is seeking a dedicated professional to join our team as an R&D Assistant.
What you will do:
The R&D Assistant will support the development, optimization, and verification of rapid diagnostic test kits and related in vitro diagnostic (IVD) products. This role is hands-on and laboratory-focused, involving experimental work, documentation, and coordination with cross-functional teams. The ideal candidate is detail-oriented, organized, and eager to grow within biotechnology/diagnostics environment.
Key Responsibilities
Laboratory Work & Experimentation
Perform laboratory experiments related to immunoassays, rapid diagnostic tests, and associated reagents.
Conduct sample preparation, reagent handling, and routine lab procedures under established protocols.
Record experimental data accurately and maintain complete, traceable lab notebooks.
Method Development & Optimization
Assist in the development and optimization of assay procedures, workflow steps, and prototype evaluations.
Support troubleshooting activities and contribute observations during feasibility and development studies.
Verification & Validation (V&V) Support
Participate in product verification, validation, and performance testing (analytical/clinical simulations).
Ensure all testing activities follow SOPs, regulatory requirements, and quality system guidelines.
Documentation & Technical Writing
Prepare technical documents including SOPs, experimental protocols, V&V reports, stability logs, and R&D records.
Maintain and update R&D documentation in compliance with ISO 13485 and internal QMS requirements.
Cross-Functional Collaboration
Work with Quality, Production, and Technical teams to support technology transfer activities.
Assist with drafting process instructions and providing clarification to production personnel during scale-up.
Laboratory Operations
Maintain lab equipment, perform basic troubleshooting, and arrange calibration/maintenance when needed.
Monitor consumables inventory, manage reagent preparation, and support general lab organization to ensure efficient workflow.
Qualifications
Required
2-3 years of hands-on laboratory experience in immunoassays, biochemistry, microbiology, or related wet-lab techniques.
Familiarity with pipetting, basic analytical equipment, and standard lab safety practices.
Experience preparing technical documentation: SOPs, protocols, experiment records, and data summaries.
Ability to work independently with good time-management and strong attention to detail.
Education
Master's degree or above in Life Sciences (Biochemistry, Biotechnology, Biology, Microbiology, or related fields).
Preferred
Knowledge of lateral flow assays, ELISA, or rapid diagnostic test development.
Experience working in a regulated environment (ISO 13485, GMP, or similar).
Proficiency in Mandarin preferred.
Job Type: Full-time
Pay: $22.00-$25.00 per hour
Benefits:
Dental care
Life insurance
On-site parking
Paid time off
Work Location: In person
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