About ANGLE: ANGLE is a world-leading liquid biopsy company commercialising a patent protected platform technology that can capture rare circulating tumour cells (CTCs) from blood, in a minimally invasive way, for downstream analysis. ANGLE's Parsortix® system is FDA cleared for its intended use in metastatic breast cancer and is currently the first and only FDA cleared medical device to harvest intact circulating cancer cells from blood. Parsortix technology comprises a microfluidic device that captures CTCs from blood based on their size and compressibility. CTCs are cancer cells that have detached from the primary tumour and entered the blood circulation, and they play a critical role in initiating metastasis. Once harvested, the CTCs can be comprehensively analysed to provide a wealth of information about the patient’s tumour, advancing cancer research and potentially personalized medicine. This technology has the potential to deliver profound improvements in clinical and health economic outcomes. ANGLE has established a CTC harvest and analysis service from our UK-based Clinical Laboratory based in Guildford for customers worldwide. In alignment with company priorities, we plan to rapidly expand our services to include molecular profiling of CTCs and ctDNA using digital PCR and NGS to add to our image-based assays. Join our Team: This is an exciting time at ANGLE and our team in Guildford are looking for a Programme Manager, to lead and coordinate projects within the New Product Development (NPD) and New Product Introduction (NPI) processes for ANGLE. At ANGLE, we foster a dynamic, entrepreneurial approach to translating leading-edge translational research into clinical diagnostics. We promote a culture of collaboration and shared excellence while encouraging an open and honest exchange of ideas. We are always in search of potential employees who share our vision and want to make a difference today. In your submission, please describe your background and what you can bring to our team along with attaching your resume. Principal Accountabilities: The ideal candidate will work cross-functionally, ensure regulatory compliance, and drive the delivery of products and services from concept to market. This role requires exceptional programme management skills, knowledge of medical device and biotech development processes, and a strong focus on delivering high-quality, compliant products. Define, plan, and execute programme objectives to deliver New Product Development projects on time, within budget, and to quality standards. Develop comprehensive programme plans, including timelines, budgets, risk management, and resource allocation. Lead collaboration between R&D, quality, regulatory, clinical, manufacturing, product management and commercial teams to ensure seamless execution of NPD projects. Act as a central point of communication for all programme-related activities, fostering transparency and alignment across teams. Support technology transfer activities from development to manufacturing to commercialisation. Ensure all programme activities adhere to applicable regulatory standards (e.g., FDA, ISO 13485, MDR). Work closely with regulatory and quality assurance teams to support product submissions and audits. Maintain documentation in compliance with Design Control and Quality Management Systems (QMS). Identify programme risks and implement mitigation strategies to address potential challenges. Collaborate with product management to ensure readiness for commercialisation, including documentation, marketing collateral, and training materials. Support the smooth transition of new products into production and post-market phases. Evaluate and enhance processes for efficiency, speed, and quality. Implement best practices for programme and project management within the organisation. Qualifications, Experience, Knowledge and Attributes: Bachelor’s degree in Life Sciences, Engineering, or a related field. A Master’s degree (e.g., MBA, MSc) is preferred Certifications such as PMP, PgMP or Agile Scrum Master are preferred 3-5 years of programme or project management experience, preferably in the medical device industry Demonstrated expertise in managing New Product Development projects within regulated environments Familiarity with medical device development processes, including Design Controls, Risk Management, and Product Lifecycle Management Proficiency in programme and project management tools (e.g., Monday, MS Project, Smartsheet, Jira) Preferably experience with Lean, Six Sigma or process improvement methodologies Strong understanding or regulatory and quality requirements (e.g., FDA, ISO 13485) Knowledge of clinical trial processes and post-market surveillance is preferred Excellent organisational and communication skills A strategic thinker and planner with problem-solving and decision-making abilities Ability to manage and communicate with stakeholders Ability to manage multiple projects simultaneously and prioritise effectively Ability to collaborate and demonstrate cross-functional leadership An eye for detail and commitment to high quality data A flexible, can-do approach to the requirements of the job Results-orientated and takes accountability Job Requirements: Due to the nature of the role, our requirement is for this position to be office based in Guildford, with flexibility to work from home at the discretion of the Manager. As a member of our highly skilled team you will receive opportunities for training and development and a competitive b enefits package. Please let us know if you require disability-related accommodation during the recruitment process so that we can work with you to meet your needs. Furthermore, please be advised that if you submit an application to us for this position, your application and personal details will be processed in accordance with our Data Privacy Notice for Job Candidates. Important notice to Employment Businesses/ Agencies: ANGLE does not accept referrals from employment businesses and/or employment agencies in respect of the vacancies posted on this site. All employment businesses/agencies are required to contact our ANGLE recruitment team to obtain prior written authorisation before referring any candidates. In the absence of such written authorisation being obtained any actions undertaken by the employment business/agency shall be deemed to have been performed without the consent or contractual agreement of ANGLE. ANGLE shall therefore not be liable for any fees arising from such actions or any fees arising from any referrals by employment businesses/agencies in respect of the vacancies posted on this site.