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Thomas Gallagher
Life Science

+353870612325
[email protected]
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Details

Senior Operations Manager


Reference:TG - Senior Ops Manager Location: Dublin
Dublin City Centre
Dublin Greater
Dublin North
Dublin South
Dublin West
Kildare
Kilkenny
Laois
Leinster
Longford
Louth
Meath
Midlands
Qualification:DegreeExperience:5-7 Years
Job Type:PermanentSalary: Not Disclosed
May be suitable for: BD Manager, QA Director, QA Engineer, QA Executive, QA Manager, QA RA Engineer, QA Specialist, QA Supervisor

Role: Senior Operations Manager
Location: Cherrywood, South Dublin (Hybrid working, 2 days a week on site)
Benefits: Competitive salary, share options, Hybrid working


About the company:
My client are a MedTech start-up located in Dublin who create BioElectronics devices which modulate the peripheral nervous system in order to address many of the world’s most pressing healthcare needs. Our purpose is to unlock the universality of BioElectronics devices in healthcare treatments.

You’ll be part of a dynamic, innovative team where your contributions will truly make a real difference in the world. Here, you won’t be just a cog in the machine; you’ll be an integral part of shaping the future of healthcare. They offer a fast-paced environment that encourages creativity and problem-solving, giving you the opportunity to directly impact patient lives and drive groundbreaking advancements in medical technology. Join us to be a pioneer in the industry, working on cutting-edge projects and seeing the tangible impact of your work on a global scale.


My client are a a multi-award winning startup who were ranked second in Europe’s flagship Innovation Award, the EIC program, which funds Europe’s most promising startups.


Responsibilities
Oversee operational activities at every level of an organization including

  • General Technical Project Management
  • Hiring and management of employees
  • Quality Assurance and documentation
  • Project Reporting and documentation
  • Partner Ecosystem Management
  • Payroll & Financial Management
  • Support overall Design History File contents and associated activity plans
  • Support clinical and regulatory submissions as required
  • Support planning and management of clinical trials

Desirable Requirements
  • Degree in Engineering or relevant field
  • 6+ years of industrial experience
  • Relevant experience in quality assurance or quality management
  • Relevant experience in project management
  • Experience in medical devices
Does this sound like your next career move? For more info forward your application to the link provided or contact me on 087 0612325 OR [email protected]