Software Engineering Director

4 days ago

WottonunderEdge, Gloucestershire, United Kingdom Renishaw PLC Full time
About the Role

We are seeking a highly skilled and experienced Software Development Manager to lead our software development team in delivering innovative solutions for neurosurgical applications.

Key Responsibilities
  • Lead and mentor a team of software engineers, providing technical guidance, feedback, and coaching.
  • Define and implement software development processes, methodologies, and best practices, ensuring compliance with regulatory and industry standards.
  • Manage software development projects from initiation to closure, ensuring timely delivery, scope adherence, and customer satisfaction.
  • Design, develop, test, and deploy software solutions for medical devices using agile and iterative methods.
  • Troubleshoot and resolve software issues, ensuring high quality and reliability of software products.
  • Conduct code reviews, audits, and quality assessments, ensuring adherence to coding standards and guidelines.
  • Research and evaluate new technologies, tools, and frameworks, recommending improvements and innovations.
  • Communicate and collaborate with managers, engineers, product owners, and stakeholders to ensure alignment with the company's vision and goals.
Requirements
  • Bachelor's degree or higher in Computer Science, Engineering, or a related field.
  • At least five years of experience in software development, preferably in the medical device industry or a regulated environment.
  • Strong knowledge of image processing algorithms, techniques, and tools such as OpenCV, MATLAB, or TensorFlow.
  • Proficiency in programming languages such as C#, C++, Python, or Java, and software development methodologies like Agile or Scrum.
  • Experience in leading, managing, and mentoring software development teams, including setting goals, conducting performance reviews, and resolving conflicts.
  • Excellent communication, collaboration, and problem-solving skills, with the ability to work effectively with internal and external stakeholders.
  • Familiarity with medical device regulations, standards, and best practices such as ISO 13485, IEC 62304, or FDA 21 CFR Part 11.
  • Ability to work under pressure, meet deadlines, and deliver high-quality software products that meet customer needs and expectations.

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