Seven Life Sciences

About the Company

Seven Life Sciences has been set up with a very specific ambition in mind, to become the company Pharmaceutical, Medical Devices, Biotech and Clinical companies come to and trust when in need of specific experienced professionals for permanent or contract roles, across dedicated practice areas.

We are specialists in supplying senior individuals and teams of people worldwide.
With industry specific consultants and international offerings, we have an unparalleled network across the UK and Europe and a global reputation for expertise. Our consultants are true specialists in their niche markets; their in-depth technical knowledge and experience sets us apart from our competitors.

With a focus on specialist markets and a consistent delivery of results, Seven Life Sciences has built a lasting reputation within the Pharmaceutical & Life Sciences industry as specialist consultants with a deep understanding of the full Life Sciences development cycle.

Our network is made up of people with a high level of quality whose work history we have fully vetted, who meet our high standards and share our ambition.

We have trusted networks of professionals in:-

• Quality Assurance
• Quality Control
• Regulatory Affairs
• Medical Devices
• Specific ISO specialists
• Compliance
• Auditing
• Pharmaceutical Engineering
• Medical Device Engineering
• Validation Experts
• Computer System Validation (CSV)
• Pharmacovigilance
• Biostats
• Clinical SAS
• Clinical Operations
• Medical Affairs
• Medical Writing
• Medical Information
• Medical Scientific Liaison
• HEOR
• Labelling
• Medical Sales

Listed Jobs

Company Name

Seven Life Sciences

Job Title

Senior Software Developer

Job Description

Job Title: Senior Software Developer

Summary of the role:
Our client is aiming to bring to market a disruptive Point of Care Medical Device system which provides fast, accurate results at the point of use. As the Senior Software Developer, you will play a critical role in the development of cutting-edge medical software solutions, ensuring compliance with regulatory standards while driving technological advancements.

Responsibilities:
Design, develop, and maintain high-quality software for medical devices, ensuring safety, performance, and regulatory compliance.
Manage the software development lifecycle of the product
Collaborate with cross-functional teams, including hardware engineers, regulatory experts, and clinical specialists, to develop robust and scalable software solutions.
Lead the software development lifecycle, from requirements analysis and architecture design to implementation, testing, and deployment.
Ensure compliance with FDA, IEC 62304, ISO 13485, ISO 27001 and other medical software regulations.
Perform risk analysis, validation, and verification of software components.
Optimize software for reliability, efficiency, and scalability in embedded and cloud-based medical systems.
Provide mentorship and technical guidance across the business

Education required: Bachelor's or master's degree in computer science, Software Engineering, Biomedical Engineering, or a related field.

Experience:
5+ years of experience in software development, preferably within the medical devices industry.
Proficiency in C, C++, Python, or Java, with a strong understanding of software architecture and design patterns.
Experience with embedded systems, real-time operating systems (RTOS), and cloud-based medical software solutions.
Familiarity with medical software regulations and standards (IEC 62304, FDA 21 CFR Part 820, ISO 13485, ISO 14971).
Strong problem-solving skills and ability to work in a collaborative environment.
Experience with AI/ML applications in medical devices.
Knowledge of cybersecurity best practices for healthcare applications.
Understanding of wireless communication protocols (Bluetooth, Wi-Fi) and IoT applications in medical technology.
AWS experience a distinct advantage

Location of role: Scotland - Remote

Scotland, United Kingdom

Remote

11-03-2025