Shifamed

Principal Mechanical Design Engineer

Shifamed

Doha, Doha Municipality, Qatar · Full Time

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Experience
15+ yrs
Salary
Openings
1
Posted
1 week ago
Work mode
In office
Education
Bachelor's Degree or higher in Mechanical/Biomedical Engineering
Eligibility
Experienced mechanical/biomedical engineering professionals with a strong medical device background, particularly those who have led regulated product development programs and can work on-site in Doha, Qatar.
Resume
Required to apply

Where you'll work

Job description

Role overview

This opportunity is with Akura Medical, part of the Shifamed portfolio, a company building a differentiated treatment platform for venous thromboembolism (VTE). Akura has received US IDE approval for the QUADRA-PE study of the Katana™ Thrombectomy System for acute pulmonary embolism, and is also creating NavIQ™, a software solution that converts CT angiograms into 3D pulmonary vascular models to improve visualization, procedural planning, clot assessment, safety, effectiveness, and usability. The company recently completed a $53 million first close of its Series C round, led by the Qatar Investment Authority, to support a joint venture and a new R&D and manufacturing center in Doha, Qatar.

Shifamed, founded in 2009 by serial entrepreneur Amr Salahieh, is a privately held medical device innovation hub focused on creating novel products for cardiology and ophthalmology.

This is a full-time, on-site role in Doha, Qatar, for a principal-level mechanical design engineer who will help shape a blood clot removal system from early concept through high-volume manufacturing. The position involves designing consumable and capital equipment components, working closely with vendors and cross-functional partners, and supporting testing and documentation aligned with applicable standards.

What you'll do

  • Own the design and development of plastic, composite, and metal parts from initial concept through high-volume production, including DFM/DFS work and coordination with suppliers on manufacturing and tooling choices.
  • Manage the full mechanical development cycle, covering requirements definition, concept generation, prototyping, detailed design, verification and validation, and transfer into production.
  • Work across mechanical, electronic, firmware, fluid, and user-interface elements with multidisciplinary teams to create integrated product solutions.
  • Perform and guide engineering analysis such as tolerance studies, finite element analysis, material selection, and root-cause investigations for critical subsystems.
  • Create practical and inventive product concepts that address unmet clinical needs in thrombectomy.
  • Contribute to the company’s intellectual property strategy through invention disclosures and prototype work that demonstrates reduction to practice.
  • Engage with physicians to support product demonstrations and testing activities.
  • Maintain thorough development records through design reviews, manufacturing instructions, test procedures, and test reports.
  • Support supplier selection and management by evaluating capabilities, materials, and fabrication methods.
  • Participate in lab and cleanroom builds, process optimization, and design-of-experiments work supported by statistical methods.
  • Assist with regulatory submissions by drafting technical content and providing engineering input.
  • Mentor less experienced team members and contribute effectively both independently and within project teams.

Requirements

  • A bachelor’s degree or higher in Mechanical Engineering, Biomedical Engineering, or a closely related field.
  • At least 15 years of experience in complex product development, including work on regulated products.
  • Strong command of SolidWorks, with advanced-level proficiency.
  • Proven background as a lead or principal engineer on medical device design projects from concept to launch.
  • Deep experience with injection molding and RIM molding, including part design, material selection, DFM, and cosmetic and structural considerations.
  • Strong understanding of medical device development under FDA, ISO 13485, or comparable regulatory systems.
  • Hands-on experience with clinical testing, trials, data collection, and statistical analysis.
  • Experience in designing durable electromechanical mechanisms and higher-volume disposable components.
  • Practical exposure to molding, machining, prototyping, pilot production, and fixture/tool design.

Additional information

The compensation range is determined based on role level and location, and the final offer will also reflect job-related knowledge, geographic location, skills, experience, education, and relevant certifications or training.

Notice to candidates

This employer does not conduct interviews or issue job offers through mobile web chat applications. Any such activity should be reported to hr@shifamed.com.

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