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Programme Manager - Job Opportunity at ANGLE plc

Guildford, United Kingdom
Full-time
Mid-level
Posted: February 5, 2025
Hybrid
GBP 65,000 - 85,000 per year based on location and role requirements

Benefits

Competitive benefits package with training and development opportunities
Flexible work arrangement with hybrid option
Professional development support
Healthcare coverage (implied based on company size and location)
Pension scheme (standard for UK companies)

Key Responsibilities

Lead end-to-end program management for medical device development from concept to commercialization
Direct cross-functional collaboration between R&D, quality, regulatory, clinical, manufacturing and commercial teams
Ensure regulatory compliance and quality standards adherence
Manage technology transfer and commercialization processes
Oversee risk management and mitigation strategies
Drive process improvement and efficiency initiatives

Requirements

Education

Bachelor's degree in Life Sciences, Engineering, or related field. Master's degree preferred

Experience

3-5 years of programme or project management experience

Required Skills

Medical device development expertise Design Controls knowledge Risk Management proficiency Product Lifecycle Management Programme and project management tool proficiency Strong organizational and communication skills Strategic thinking and planning Stakeholder management Multi-project management Cross-functional leadership

Certifications

PMP PgMP Agile Scrum Master (preferred)
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Sauge AI Market Intelligence

Industry Trends

Growing demand for liquid biopsy technologies in cancer diagnostics and personalized medicine Increasing regulatory scrutiny in medical device development requiring specialized program management expertise Rising importance of cross-functional integration in medical device development Shift towards digital transformation in healthcare technology development processes

Role Significance

Likely coordinating with 15-20 team members across multiple functional areas
Mid to senior-level position with significant influence on product development success and commercial outcomes

Key Projects

Medical device regulatory submissions and approvals Technology transfer initiatives Quality management system implementation New product development lifecycle management Commercial launch preparations

Success Factors

Deep understanding of medical device regulatory landscape Ability to balance technical, regulatory, and commercial requirements Strong stakeholder management across multiple disciplines Effective risk management and mitigation strategies Clear communication and documentation practices

Market Demand

High demand due to specialized nature of medical device program management and growing biotech sector in UK

Important Skills

Critical Skills

Medical device regulatory knowledge due to FDA and ISO compliance requirements Program management expertise for complex multi-stakeholder projects Technical understanding of medical device development processes Quality management system experience

Beneficial Skills

Experience with clinical trials Knowledge of cancer research and diagnostics Digital PCR and NGS understanding Commercial launch experience

Unique Aspects

Opportunity to work with first FDA-cleared CTC capture technology
Direct impact on cancer research and personalized medicine advancement
Complex regulatory and technical environment requiring specialized expertise

Career Growth

2-3 years in role before advancement, depending on project success and organizational growth

Potential Next Roles

Senior Programme Manager Head of Product Development Director of Operations Technical Program Director

Company Overview

ANGLE plc

ANGLE plc is a pioneering liquid biopsy company with FDA-cleared technology for CTC capture and analysis

Leading position in specialized medical device market with unique FDA-cleared technology
Strong UK presence with global commercial reach
Innovation-focused environment with emphasis on scientific excellence and regulatory compliance
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