Program Manager in Chester

Program Manager in Chester

Chester Full-Time 60000 - 80000 Β£ / year (est.) No working from home possible
Spacelabs Healthcare

At a Glance

  • Tasks: Lead innovative healthcare projects from concept to completion, ensuring top-notch delivery.
  • Company: Join Spacelabs Healthcare, a leader in healthcare technology innovation.
  • Benefits: Competitive salary, career growth, and the chance to make a real impact.
  • Other info: Dynamic team environment with opportunities for international travel.
  • Why this job: Be at the forefront of healthcare innovation and improve patient outcomes globally.
  • Qualifications: 6+ years in R&D with strong leadership and project management skills.

The predicted salary is between 60000 - 80000 Β£ per year.

At Spacelabs Healthcare, we are on a mission to provide continuous innovation in healthcare technology for better clinical and economic outcomes. Our scalable solutions deliver critical patient data across local and remote systems, enable better-informed decisions, increase efficiencies, and create a safer environment for patients.

We are seeking a Program Manager to join our Diagnostic Cardiology team in Edinburgh. This team is responsible for developing new products and enhancing existing ones across a portfolio of electronic medical devices, application software, and accessories. As Program Manager, you will lead global, cross-functional teams through the entire product lifecycle from concept and development to manufacturing and ongoing maintenance. This is a high-impact role requiring strong leadership, technical expertise, and a passion for delivering innovative healthcare solutions.

Responsibilities:

  • Drive new product development programs from concept to completion, ensuring delivery on time and within budget.
  • Lead and mentor project teams, enforcing best practices and compliance with company policies and regulatory standards.
  • Develop detailed project plans, requirements, specifications, schedules, and risk analyses.
  • Negotiate trade-offs between schedule, resources, and product features.
  • Ensure adherence to ISO13485, FDA CFR 820:30, and IEC 62304 standards.
  • Provide regular updates and formal reviews to senior management and stakeholders.
  • Manage contract resources and ensure quality deliverables.
  • Uphold Spacelabs core values: Integrity, Innovation, Accountability, and Teamwork.

Requirements:

  • Education: Bachelors degree in Engineering, Computer Science, or related field (Masters preferred).
  • Experience: 6+ years in R&D roles, including Program/Project Management.
  • Proven track record leading cloud software platform development with hardware integration.
  • Familiarity with embedded systems, APIs, and firmware integration.
  • Strong knowledge of medical device regulations (FDA, EUMDR) and quality systems.
  • Excellent leadership, communication, and negotiation skills.
  • Highly proactive, detail-oriented, and able to anticipate and mitigate risks.
  • Proficiency in Microsoft Project and advanced MS Office skills.
  • Ability to work across global time zones and travel internationally.

Desirable Skills:

  • Experience with IEC 60601 standards and ISO14971 risk management.
  • Participation in Notified Body audits or technical file reviews.

Program Manager in Chester employer: Spacelabs Healthcare

At Spacelabs Healthcare, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters innovation and collaboration in the heart of Edinburgh. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment that encourages professional development. Join us to be part of a mission-driven team dedicated to improving healthcare technology, where your contributions will directly impact patient outcomes and safety.

Spacelabs Healthcare

Contact Details:

Spacelabs Healthcare Recruitment Team

We think you need these skills to ace Program Manager in Chester

Program Management
Leadership Skills
Technical Expertise
Project Planning
Risk Analysis
ISO 13485
FDA CFR 820:30