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Technical Coordinator, R&D (Medical Devices)

20 800
Формат работы
onsite
Тип работы
fulltime
Английский
c1
Страна
Malta
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Technical Coordinator, R&D (Medical Devices): Supporting lifecycle and sustaining activities for Medication Delivery products with an accent on supplier changes, end-of-life initiatives, labelling design changes, and quality systems. Focus on coordinating cross-functional operational work, maintaining KPI tracking, and driving continuous improvement in a regulated medical device environment.

Location: Marsa, Malta; onsite, full time

Salary: €20,800 minimum annually, with potential for higher pay based on skills, expertise, and experience. The position may also include benefits, discretionary bonuses, and/or long-term incentives.

Company

hirify.global develops healthcare products and solutions with a mission to save and sustain lives.

What you will do

  • Coordinate sustaining and lifecycle activities for the Medication Delivery portfolio, including supplier change notifications, change control records, product code obsolescence, and end-of-life initiatives.
  • Support labelling design changes, including redlines, label verifications, and related standard work activities.
  • Contribute to market enhancements, manufacturing activities, product design improvements, and continuous improvement initiatives.
  • Maintain metrics and tracking systems for operational activities and critical KPIs.
  • Apply quality systems and relevant corporate, divisional, and departmental procedures.

Requirements

  • A-Level or diploma in a technical or science-based subject.
  • Flexibility to shift between projects and manage multiple priorities.
  • Self-motivated, resourceful, and able to work autonomously while contributing as a team member.
  • Strong interpersonal and communication skills for working with internal and external customers.
  • Fluent English required.

Culture & Benefits

  • Work in a regulated medical device environment focused on quality and operational efficiency.
  • Collaborative culture built around courage, trust, ownership, and accountability.
  • Potential eligibility for competitive benefits, discretionary bonuses, and/or long-term incentives.
  • Reasonable accommodations are available for candidates with disabilities during the application and interview process.

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