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Apex Systems

Staff Engineer

Toronto, ON, Canada

Pay: $42 to $50 USD / hour
Job type: Contract
Apply by: Oct 22, 2026
Posting language: English
Posted: Sep 22, 2026

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Original job description

Job#: 3044035

Job Description:

Medical Device Development - Engineer III

Client: Biotechnology company

Contract/Perm & duration: 12-month contract

Location: Downtown Toronto, this position will be working 4-5 days onsite per week.

Pay Rate: $42-50/hr

Responsibilities:

Assist in the design of cutting-edge regenerative medicine delivery systems while determining own tasks and appropriate sequence of activities.
Create engineering documentation (dwg, specs, BOMs, assembly instructions, inspection forms, etc.)
Develop manufacturing processes for medical devices, components and subassemblies, coordinate prototype and test builds internally and with 3rd party vendors
Set device and system requirements; create CAD models, prototypes, and design iterations.
Define design phase gate activities (e.g. design freeze, design V&V, etc.) to advance device development.
Support the development of intellectual property – invent new technologies, write invention disclosures, aid in preparation of patent filings.
Author and execute design verification and validation protocols; analyze results and prepare reports.
Communicate effectively with fellow engineers and non-technical personnel. Write memos, protocols, reports as well as prepare and give presentations.
Work effectively in cross-functional teams with colleagues in a wide range of areas including cell biology, manufacturing (in-house and third party), quality, regulatory affairs, clinical development, surgery and interventional medicine.
Collaborate closely with Supply Chain, Quality, and Operations to ensure smooth flow of daily work. Execute pilot manufacturing operations when needed to ensure smooth flow of daily work.
Support and collaborate with suppliers, including third party manufacturers.
Support and execute design verification testing – pay close attention to detail to ensure compliance to protocols and accurately record data.
Identify and implement new R&D tools, test methods, and equipment as needed.
Other duties as assigned.

Key Qualifications:

Biomedical or Mechanical Engineering degree, or relevant Engineering degree with a minimum of 4+ years (2 + if Master’s Degree) experience in medical device development with a focus on R&D
Knowledge of design control systems such as ISO 13485 and FDA Quality System Regulation (21 CFR 820)
Proficiency with 3D modeling software, SolidWorks preferred
Experience with drafting DHF and DMR documentation
Strong experimental design and statistical analysis skills
Hands-on skills such as – prototype assembly, fabrication and design iterations
Demonstrated analytical skills, especially in the areas of process improvement, problem solving, and logical thinking
Highly developed organizational skills able to handle multiple high priority tasks/projects concurrently.
Excellent interpersonal, verbal and written communication skills
Comfortable in a fast-paced small company environment with minimal direction and able to adjust workload based upon changing priorities
Ability to work independently or in teams
Demonstrated enthusiasm and willingness to learn

Everforth Apex is a world-class IT services company that serves thousands of clients across the globe. When you join Everforth Apex, you become part of a team that values innovation, collaboration, and continuous learning. We offer quality career resources, training, certifications, development opportunities, and a comprehensive benefits package. Our commitment to excellence is reflected in many awards, including ClearlyRateds Best of Staffing® in Talent Satisfaction in the United States and Great Place to Work® in the United Kingdom and Mexico.

Everforth Apex Benefits Overview: In terms of professional development, Everforth Apex hosts an on-demand training program, provides access to certification prep and a library of technical and leadership courses/books/seminars once you have 6+ months of tenure, and certification discounts and other perks to associations that include CompTIA and IIBA.

© 2026 Everforth, Inc. All rights reserved.

Everforth Apex Systems is part of the Commercial Segment of Everforth, Inc.

NYSE: EFOR

4400 Cox Road

Suite 200

Glen Allen, Virginia 23060

Everforth Apex is an equal opportunity employer. We do not discriminate or allow discrimination on the basis of race, color, religion, creed, sex (including pregnancy, childbirth, breastfeeding, or related medical conditions), age, sexual orientation, gender identity, national origin, ancestry, citizenship, genetic information, registered domestic partner status, marital status, disability, status as a crime victim, protected veteran status, political affiliation, union membership, or any other characteristic protected by law. Everforth Apex will consider qualified applicants with criminal histories in a manner consistent with the requirements of applicable law. If you have visited our website in search of information on employment opportunities or to apply for a position, and you require an accommodation in using our website for a search or application, please contact our Benefits Department at [email protected] or 804-523-8228. (Do not submit resumes or solicit consultants to this email address). UnitedHealthcare creates and publishes the Transparency in Coverage Machine-Readable Files on behalf of Everforth Apex.

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More about this job

Responsibilities

The engineer will design regenerative medicine delivery systems, develop manufacturing processes, and create engineering documentation including CAD models and prototypes. They will also execute design verification and validation protocols while collaborating with cross-functional teams in quality, regulatory, and clinical development.

Requirements

Candidates must hold a degree in Biomedical or Mechanical Engineering with at least 4 years of experience in medical device R&D. Proficiency in design control systems like ISO 13485 and FDA regulations, along with strong 3D modeling skills, is required.

Skills

Medical device development
R&D
ISO 13485
FDA Quality System Regulation
SolidWorks
3D modeling
Engineering documentation
Manufacturing processes
CAD
Design verification
Design validation
Experimental design
Statistical analysis
Prototype assembly
Problem solving
Process improvement

Benefits

Training program
Certification preparation
Technical and leadership courses
Certification discounts

Visa sponsorship

Not detected in the job text

Keywords

Medical Device
Regenerative Medicine
R&D
ISO 13485
FDA 21 CFR 820
SolidWorks
CAD
DHF
DMR
BOM
Design Verification
Design Validation
Statistical Analysis
Prototyping
Manufacturing
Quality Assurance
Regulatory Affairs
Biomedical Engineering
Mechanical Engineering
Intellectual Property
Patent Filings
Supply Chain
Operations
Process Improvement
Cross-functional Teams

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