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Human factors specialist

Coleraine
Permanent
Eakin Healthcare
€60,000 a year
Posted: 23 December
Offer description

WHY JOIN US?

We’re good at what we do – come and join us and you can benefit from:

* Blended Working
* Bonus
* 25 days holiday plus bank holidays (rising to 28)
* Option to buy holiday days
* Health Cash Plan
* Pension
* Life Assurance
* Enhanced Maternity/Paternity
* Cycle to Work Scheme
* Referral Scheme
* Long Service Awards
* Free Parking


ABOUT THE ROLE

Reporting to the Head of Clinical and Regulatory Affairs, this is an exciting opportunity to play an important role within Eakin Healthcare. Expansion and diversification of our product portfolio necessitates an experienced Human Factors Specialist to support the team in developing innovative medical devices and MDR remediation. Working closely with our Research and Development, and Commercial teams, you will be responsible for managing multiple projects within the Eakin Healthcare portfolio. Ideally this role will be based at our Coleraine site. However, remote working options with monthly on‑site visits may be considered.


KEY RESPONSIBILITIES


Human Factors activities

* Develop pragmatic Human Factors strategies for new and ongoing projects that ensure alignment with regulatory compliance.
* Utilise in‑depth understanding of Human Factors principles, user needs and regulatory frameworks to plan and deliver high quality Formative and Summative studies with limited guidance.
* Confidently plan and deliver high quality documentation for a range of Human Factors activities, including and not limited to Expert reviews, Use‑related Risk Analysis, Known Use Issues Reports and Threshold Analysis Reports for medical devices.
* Actively influence new product design by generating and validating user requirements.
* Champion the development of established and new processes to keep internal practices up to date.


Regulatory compliance and documentation

* Remain up to date with impending changes and developments regarding regulatory compliance.
* Provide support to enhance internal understanding of MDR regulations, ISO13485, ISO14971, IEC62366 and FDA Human Factors regulations.


Collaboration and Stakeholder Engagement

* Collaborate with R&D, Marketing and QA/RA functions within the Eakin Healthcare Group and provide Human Factor support as required.
* Raise awareness and understanding of Human Factors principles internally within the company through actively promoting the discipline and being seen as a subject matter expert that others turn to for guidance and expertise.


Other

* To adhere to the company’s Equal Opportunities policy and Dignity at work policy in all activities and to actively promote equality of opportunity wherever possible
* To be responsible for your own health and safety and that of your colleagues, in accordance with the company’s Health and Safety policy
* To adhere to the company’s Quality policy and Environmental policy
* To undertake other duties as may be reasonably required


WHAT WE’RE LOOKING FOR

* 4+ years of experience in leading full Human Factors programmes in the field of medical devices.
* Expert understanding of Human Factors as a discipline, including documentation, studies, and best practices.
* Experience in championing HF and usability, ensuring it is kept at the core of product development.
* Mentoring colleagues in the application of Human Factors techniques and approaches during product development.
* An understanding of up‑to‑date regulatory frameworks surrounding medical device development, including IEC62366 and FDA Human Factors regulations.
* Degree educated in a relevant discipline.
* Experience with Class IIa and Class IIb respiratory medical devices.


KEY WORKING RELATIONSHIPS


Internal

* Working with Operations, Regulatory and the R&D team to support Human Factors activities and provide advice and support to peers
* Collaborating with Commercial functions across Eakin Healthcare Group to support gathering of usability data for market launch and on‑going device marketing activities
* Group wide QA/RA functions to provide clinical support for continuous improvement


External

* End‑users
* Regulatory bodies
* Research agencies


ADDITIONAL INFORMATION

* Ability/willingness to develop within the role
* Ability/willingness to attend training courses in relation to the role and the needs of the department
* Ability/willingness to travel to other Eakin Group sites as needed


COMPETENCIES


Customer Focus

Building strong customer relationships and delivering customer‑centric solutions.


Global Perspective

Taking a broad view when approaching issues, using a global lens.

Knowing the most effective and efficient processes to get things done, with a focus on continuous improvement.


Builds Networks

Effectively building formal and informal relationship networks inside and outside the organization.


Values Differences

Recognising the value that different perspectives and cultures bring to an organisation.


Communicates Effectively

Developing and delivering multi‑mode communications that convey a clear understanding of the unique needs of different audiences.

Gaining the confidence and trust of others through honesty, integrity and authenticity.


Nimble Learning

Actively learning through experimentation when tackling new problems, using both successes and failures as learning fodder.


Seniority level

* Mid‑Senior level


Employment type

* Full‑time


Job function

* Product Management and Research


Industries

* Medical Equipment Manufacturing
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