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Senior project lead - medical device industry

Dublin
beBeeprogrammanagement
Industry
Posted: 31 July
Offer description

Program Manager Job Description

We are seeking an experienced and motivated Program Manager to oversee and drive the success of strategic projects and initiatives within the medical device industry.

This role requires both technical expertise and a strong understanding of quality and regulatory standards within the medical device industry.

The successful candidate will have 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).

* Lead and manage multiple programs that span the lifecycle of medical device development, from ideation through design, development, and regulatory approval
* Cross-functional Collaboration with product development, engineering, quality assurance, regulatory affairs, and commercial teams to ensure successful program execution
* Regularly communicate program progress, risks, and milestones to senior management and key stakeholders
* E nsure that expectations are properly set and managed across all involved parties
* Regulatory Compliance with relevant requirements (e.g., FDA, CE, ISO), managing documentation, testing, and approvals needed for device market entry
* Quality Control to ensure the product meets the highest industry standards, regulatory requirements, and customer expectations
* Resource Allocation to manage resources effectively across multiple projects
* Budget and Schedule Management to monitor and control program budgets, providing financial oversight
* Team Leadership to lead and mentor cross-functional teams, promoting collaboration, accountability, and a high-performance culture


Required Skills and Qualifications

Experience in hearing technology or similar industries is highly desirable.

Educated to degree level in Biomedical Engineering, Mechanical Engineering, Life Sciences, or a similar related field.

PMP (Project Management Professional), PgMP (Program Management Professional), or similar certifications are advantageous.

Familiarity with ISO 13485, FDA regulations, and other relevant industry standards is beneficial.


What We Offer

A competitive salary, healthcare benefits, and hybrid working arrangements in a dynamic and rapidly evolving medical device environment.

A global perspective and mindset with the ability to work effectively in multi-disciplinary teams.

A commitment to quality and a willingness to travel internationally as required.

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