Skip to main content
Post your CV and find your next job on Indeed!

Medical Device jobs in Northern Ireland

Sort by: -
    • Maintain and develop full regulatory compliance for medical device manufacturing under ISO 13485 and MHRA guidelines.
    • ISO 13485: 1 year (preferred).
    • Registered Nurse background or previous medical device training experience would be highly advantageous.
    • Strong training experience, ideally within diagnostics,…
    • Private medical and dental insurance.
    • This role contributes to the development and maintenance of data-driven solutions that improve business decision making.
    • View all Allstate jobs - Belfast jobs - Data Scientist jobs in Belfast
    • Salary Search: Data Scientist Consultant II - (Hybrid) salaries in Belfast
    • See popular questions & answers about Allstate
    • Ideally sales or clinical experience within the medical device industry.
    • In this role, you will promote and sell Medtronic’s CRDN portfolio, including coronary…
    • Previous medical device, capital equipment or healthcare technology sales experience would be an advantage.
    • Identify and develop new business opportunities for…
    • Assemble, test, and package medical devices by following clearly defined work instructions and standard processes.
    • Experience with data handling and analysis in automated experiments (e.g. logging device data, handling experimental metadata, basic analysis or visualization).
    • As a senior member of the Global Notifications team, you will work closely with the Business Unit lead to provide strategy, leadership and guidance to industry…
    • Experience within medical devices, scientific instrumentation or current/ex military engineers.
    • Carry out planned preventative maintenance on endoscopy and…
    • Private medical insurance for your peace of mind.
    • This is a full-time role, combining remote working with travel to GP practices as required.
    • Experience within medical devices, scientific instrumentation or other complex electro-mechanical equipment is advantageous.
    • Working on a production line, manufacturing medical devices.
    • Training will be provided onsite!
    • Pay Rate: *Day shift: £13.30 Evening shift: £15.96.
    • Experience within a pharmaceutical, medical device, or regulated manufacturing environment.
    • The Engineering Department Administrator is responsible for…
    • Develop and execute sales strategies to increase market share and stimulate market growth for the ruminant portfolio.
    • Ensure all dental devices meet health standards, safety regulations, and quality assurance protocols.
    • In this vital role, you will fabricate, repair, and…

People also searched:

medical service engineer

Job Post Details

Regulatory and Compliance Manager - Medical Device Manufacturing - job post

Quoris3D
17 Tully Road, Enniskillen BT94 1RL
£32,000 - £50,000 a year - Permanent, Full-time

Job details

Pay

  • £32,000 - £50,000 a year

Job type

  • Permanent
  • Full-time

Location

17 Tully Road, Enniskillen BT94 1RL

Full job description

Position Overview

We are seeking a dedicated and experienced Regulatory and Compliance Manager to lead and maintain our company’s regulatory compliance framework across key standards and bodies, including ISO 13485, DAMAS, and the MHRA. As a medical device manufacturer, we require an individual who has proven experience in a similar role, preferably with knowledge of ISO 13485.

This is a pivotal role responsible for embedding compliance into the heart of our operations, contributing directly to system development, quality control, customer experience, and business integrity.

The successful candidate will also ensure compliance with medical device manufacturing requirements, particularly in relation to our Lab-to-Lab services model, where we act as both a manufacturer and supplier within the clinical and dental ecosystem.

They will additionally lead initiatives in cybersecurity compliance aligned with ISO 27001, and manage our intellectual property portfolio including patents, trademarks, and product licensing.

Key Responsibilities

Regulatory Compliance – Medical Devices & Lab-to-Lab Services

  • Maintain and develop full regulatory compliance for medical device manufacturing under ISO 13485 and MHRA guidelines.
  • Ensure robust implementation of post-market surveillance, risk management, and product traceability processes.
  • Ensure DAMAS compliance specific to dental laboratory practices and quality systems.
  • Develop and manage documentation and procedures to support regulatory requirements across our Lab-to-Lab service model.
  • Coordinate internal and external audits, ensuring readiness at all times.

Quality & Systems Development

  • Collaborate cross-functionally with R&D, Operations, Sales, and Customer Support to embed compliance and quality assurance into business processes.
  • Support continuous improvement initiatives that enhance system efficiency and customer satisfaction.
  • Lead CAPA and internal review systems in collaboration with the wider team.

Cybersecurity & Data Compliance

  • Lead the implementation and management of cybersecurity compliance aligned with ISO 27001.
  • Ensure alignment between digital systems, data protection protocols, and regulatory expectations for medical devices and patient-related data.

Intellectual Property & Legal Compliance

  • Manage and organise compliance around IP assets: patents, trademarks, and product licences.
  • Liaise with legal and R&D teams to ensure accurate registration, renewal, and protection of proprietary technologies and services.

Pay: £32,000.00-£50,000.00 per year

Ability to commute/relocate:

  • Enniskillen BT94 1RL: reliably commute or plan to relocate before starting work (required)

Application question(s):

  • Do you have experience in a regulatory or compliance role?

Experience:

  • ISO 13485: 1 year (preferred)

Work Location: In person

Let Employers Find YouUpload Your Resume