Introduction

The Senior Systems Engineer will assume a pivotal role in the conceptualization, development, testing, and documentation of intra-aortic balloon pump consoles at our company. This individual will collaborate with a diverse team of engineers and have the opportunity to make meaningful contributions to a life-saving product. They will take the lead in systems engineering-related activities for product development initiatives and demonstrate exceptional verbal and written communication skills.

What are you going to do 

  • Spearhead systems engineering initiatives for a sophisticated, software-driven medical device.
  • Lead the creation and upkeep of product specifications, requirement documents, hazard analysis documents, and other technical records.
  • Offer technical leadership throughout the phases of product design, development, integration, testing, and enhancements to reliability.
  • Collaborate with subsystem teams, domain experts, and suppliers to identify, record, evaluate, and rectify defects.
  • Work closely with a diverse technical team to generate, revise, and maintain documentation that becomes part of the product design history file (DHF).
  • Execute projects with well-defined objectives and on-time deliverables, comprehending the objectives and contents of development and research projects.
  • Serve as the technical liaison within the company, providing insights and recommendations for system verification aspects of projects.
  • Maintain open and effective communication with the project manager and team members regarding project scope, timelines, and design alterations.

Essential skills and knowledge 

  • Bachelor's degree in Systems Engineering, Biomedical Engineering, Electrical Engineering, Computer Science, or Mechanical Engineering (or equivalent in a technical/scientific field); a Master's degree is preferred.
  • Over 7 years of experience as a Systems Engineer in product design, development, and/or testing, with a preference for experience in class II medical device products.
  • Profound understanding of medical device product design and regulatory processes.
  • Proficient in verbal and written communication.
  • Familiarity with medical device design and development processes compliant with standards such as ISO 9000, ISO 13485, IEC 62304, IEC 60601, and ISO 14971.
  • Strong grasp of system design, electronics, mechanical and software integration.
  • Knowledge of design of experiments.
  • Technical expertise in best-practice product development methodologies.

What we offer

Why work with Brunel? We are proud to offer exciting career opportunities from over 100 offices globally in 42 countries. Advancing your career takes time and effort – let us match you to your ideal position.

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Application process

First Contact

We carefully review your application and in the coming weeks, you will be notified for an interview session if you are selected. Only shortlisted candidates will be contacted within 7 days.

Scheduling an Interview

After being shortlisted, you will be contacted via email or telephone to arrange for a date on your availability for the qualification interview.

Phone/ Qualification Interview

During the interview, you will be assessed on your level of experience and skills, work history, availability, and the qualifications the company is seeking for the position.

Meeting in Real Life

After successfully making through the phone interview, a face to face interview will be scheduled between the candidate and recruiter. This session can be a more in-depth  interview to review your communication and interpersonal skills.

Application for the Position

Submission of candidates resume for client’s approval and screening.

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