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Medical Device Project Coordinator

3 weeks ago

Dublin, Dublin City, Ireland beBeeProject Full time €60,000 - €80,000
Job Title: Medical Device Project Coordinator.

Are you an experienced Program Manager looking to take the next step in your career? Do you have a passion for medical device development and want to join a dynamic team?

This is a fantastic opportunity to work with a leading company in the medical device industry, overseeing the success of strategic projects and initiatives. As a Medical Device Project Coordinator, you will be responsible for managing cross-functional teams, ensuring alignment with business goals, and driving the successful delivery of innovative medical devices that enhance patient care.

Responsibilities:
  • Program Management: Lead and manage multiple programs throughout the lifecycle of medical device development, from ideation through design, development, and regulatory approval.
  • Cross-functional Collaboration: Work closely with product development, engineering, quality assurance, regulatory affairs, and commercial teams to ensure successful program execution.
  • Stakeholder Communication: Regularly communicate program progress, risks, and milestones to senior management and key stakeholders.
  • Regulatory Compliance: Ensure that all programs comply with relevant regulatory requirements (e.g., FDA, CE, ISO), managing documentation, testing, and approvals needed for device market entry.
  • Quality Control: Oversee the quality assurance processes, ensuring the product meets the highest industry standards, regulatory requirements, and customer expectations.

Qualifications:
  • Experience: At least 3 years of experience in program management, specifically within the medical device industry or a closely related field (e.g., healthcare, biomedical engineering).
  • Education: Degree in Biomedical Engineering, Mechanical Engineering, Life Sciences, or a similar related field.
  • Certifications: PMP (Project Management Professional), PgMP (Program Management Professional), or similar certifications.

Skills:
  • Strong leadership abilities and experience managing cross-functional teams.
  • Deep understanding of medical device development processes, including design control, validation, and regulatory compliance.
  • Ability to communicate effectively with diverse stakeholders, from technical teams to senior executives.

Benefits:
Competitive Salary, Healthcare + Hybrid Working, Excellent opportunity to develop your experience and career in an exciting medical device start-up company.

This role requires both technical expertise and a strong understanding of quality and regulatory standards within the medical device industry. If you are a motivated and experienced Program Manager looking for a new challenge, please apply for this exciting opportunity.