Programme Manager

Job Title: Programme Manager Medical Device

PE Global is currently recruiting for a Programme Manager on behalf of a start up Medical Device company based in Ireland. This is a permanent role with a generous salary and package.

Job Summary:

The Medical Device Programme Manager is responsible for overseeing the development and management of medical device projects from conception to market launch. This role involves coordinating cross-functional teams, ensuring compliance with regulatory requirements, and managing project timelines and budgets.

Key Responsibilities:

• Lead and manage technical, cross-functional medical device projects.
• Collaborate with internal and external teams including: R&D, regulatory, quality assurance, manufacturing and marketing teams to ensure project alignment.
• Develop, track and maintain project plans, timelines, and budgets.
• Identify and mitigate risks associated with project timelines and deliverables.
• Ensure compliance with internal QMS systems, FDA, EU MDR, ISO, and other regulatory standards.
• Conduct regular project status meetings and communicate updates to external stakeholders.
• Manage relationships with external partners and vendors.
• Prepare and present project documentation and reports.

Qualifications:

• Bachelor’s degree in Engineering, Life Sciences, or related field; Master’s degree preferred.
• Proven experience in project management within the medical device industry.
• Strong knowledge of regulatory requirements for medical devices specifically ISO13485 and ISO62304.
• Proficiency in project management tools and software.
• Certification in project management (e.g., PMP) is a plus.

Skills:

• Strong analytical and problem-solving skills.
• Strong communication skills; the ability to convey complex technical and business information clearly and effectively through presentations, documentation and meetings..
• Attention to detail and strong organizational skills.
• Ability to work collaboratively in a cross-functional team environment.

Experience:

• 8+ years of experience in project management, preferably in the medical device sector.
• Experience with product development lifecycle and regulatory submissions.

Interested candidates should submit an updated CV.

Please click the link below to apply, or alternatively send an up-to-date CV to rebecca@peglobal.net

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***