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Placements24 is seeking a Senior Biomedical Engineer to join its East London R&D team to design, develop and test next generation medical devices and systems. You will translate clinical needs into robust engineering solutions and work with clinicians, scientists and engineers to advance patient care.
The role requires 6+ years in medical device development, strong physiology knowledge, and experience with design controls, regulatory standards, and CAD/simulation tools.
Our client, a leading innovator in medical device technology, is seeking a talented Senior Biomedical Engineer to join their advanced research and development team in East London, Eastern Cape . This role is critical for the design, development, and testing of novel medical devices and systems aimed at improving patient care and diagnostic capabilities. You will work closely with a multidisciplinary team of engineers, clinicians, and scientists to translate complex biological and medical needs into functional engineering solutions. The position requires a strong foundation in engineering principles, coupled with an in-depth understanding of human physiology and medical device regulations. We are looking for a dedicated professional with a proven track record in medical device development, eager to make a significant impact in the healthcare sector. Join our client's dedicated team in East London .
Design, develop, and prototype new medical devices and instrumentation, ensuring functionality and user safety. Conduct rigorous testing and validation of devices, adhering to established protocols and regulatory requirements. Perform design verification and validation (V&V) activities, generating comprehensive documentation. Collaborate with cross-functional teams, including R&D, marketing, regulatory affairs, and manufacturing. Analyze user needs and medical requirements to define product specifications. Troubleshoot design issues and implement effective solutions throughout the product lifecycle. Ensure compliance with medical device regulations (e.g., FDA, CE marking) and quality management systems (e.g., ISO 13485). Author technical reports, design documentation, and assist in the preparation of regulatory submissions. Mentor junior biomedical engineers and contribute to the team's technical growth. Stay updated on emerging technologies and advancements in biomedical engineering and healthcare.
Bachelor's or Master's degree in Biomedical Engineering, Electrical Engineering, Mechanical Engineering, or a related field. Minimum of 6 years of experience in the design and development of medical devices or healthcare technologies. Strong understanding of human physiology, anatomy, and medical terminology. Experience with medical device design controls, regulatory requirements, and quality systems. Proficiency in relevant design software (CAD, simulation tools) and testing equipment. Excellent analytical, problem-solving, and critical thinking skills. Strong project management and organizational abilities. Effective written and verbal communication skills, with the ability to present technical information clearly. Ability to work collaboratively in a team environment and manage multiple projects. Experience in areas such as signal processing, instrumentation, or biomaterials is a plus.