- Salary
- C$50k – C$60k/yr
- Location
- Port Coquitlam, British Columbia, CA
- Type
- Full-time
- Department
- Engineering
- Source
- BetterTeam
Description
Vitacore is seeking a highly organized and detail-oriented Project Assistant – Compliance to support our product development and compliance activities across multiple projects.
- Support product development projects from initial development through verification, validation, design transfer, regulatory approval, and commercialization.
- Assist with the preparation, organization, review, and maintenance of technical and engineering documentation.
- Support design control activities, including product requirements, specifications, design inputs and outputs, verification and validation documentation, and design changes.
- Coordinate product testing with internal teams, suppliers, and external testing laboratories.
- Assist in developing test plans, protocols, reports, and supporting documentation.
- Collect, organize, review, and summarize test data and technical results.
- Track project deliverables, testing requirements, documentation, approvals, deadlines, and outstanding actions.
- Support regulatory and compliance activities, including gathering technical information and documentation required for submissions and product files.
- Assist with identifying and interpreting applicable product standards, testing requirements, and compliance requirements.
- Work with Engineering, Quality, Regulatory, R&D, and Manufacturing teams to ensure required documentation and project activities are completed accurately and on schedule.
- Support design transfer activities as products move from development into manufacturing.
- Coordinate with suppliers and external partners to obtain technical documentation, specifications, certifications, test results, and other required information.
- Maintain organized and accurate project records and documentation.
- Identify missing information, documentation gaps, outstanding testing, or other issues that may affect project timelines and proactively follow up with the appropriate stakeholders.
- Participate in project meetings and maintain clear records of decisions, action items, responsibilities, and deadlines.
- Support additional engineering, product development, compliance, and project coordination activities as required.
- Bachelor’s degree in Engineering from a recognized institution is required.
- Recent graduates and early-career engineers are encouraged to apply.
- Strong technical writing and documentation skills.
- Strong organizational skills and exceptional attention to detail.
- Ability to read, understand, and work with technical specifications, engineering documents, test results, and product requirements.
- Strong analytical and problem-solving skills.
- Ability to manage multiple priorities, deadlines, and project workstreams simultaneously.
- Strong written and verbal communication skills.
- Ability to work effectively with multidisciplinary teams.
- Proficiency with Microsoft Office, particularly Word and Excel.
- Ability and willingness to work between Vitacore's Burnaby and Port Coquitlam locations.
- Degree in Mechanical, Biomedical, Mechatronics, Materials, Chemical, Manufacturing, or another relevant engineering discipline.
- Previous co-op, internship, academic, or professional experience involving product development, testing, manufacturing, quality, or compliance.
- Familiarity with medical devices or other regulated products.
- Exposure to verification and validation, design controls, quality management systems, or regulatory documentation.
- Familiarity with technical standards, test methods, or laboratory testing.
- Experience working with engineering drawings, specifications, test protocols, or technical reports.
- $50,000 to $60,000 annual salary.
- Health & Dental benefits.
- 2 weeks paid vacation.
- Tuition Assistance Program.
- Multiple company events throughout the year.