Regulatory Affairs and QA Assistant


A new Regulatory Affairs and QA Assistant position is now available. Reporting directly to the Regulatory Affairs Manager, your responsibilities will include:

  • Assisting in implementing and ensuring compliance with medical devices regulations
  • Supporting medicinal product registrations
  • Handling post-marketing surveillance and product vigilance tasks
  • Maintaining the company’s regulatory and quality systems
  • Ensuring that the company’s quality system is in accordance with GDP standards and other applicable legislation
  • Supporting in other ad hoc duties as required by the team.

Skill-sets and Requirements

  • Excellent communication and interpersonal skills
  • Ability to work well both independently and as part of a team
  • Good planning and organization skills
  • Possess good problem solving skills

Education & Experience

  • A minimum of A’ Level standard of education in a relevant scientific or healthcare discipline
  • Knowledge of GMP/GDP standards will be considered an asset
  • Knowledge of Maltese and EU regulations and procedures will be given preference
  • Proficiency in Microsoft Office applications
  • Proficiency in both oral and written English

Job Reference: GI544

  • Primary job focus
    Quality Control
  • Job type
    Full Time
  • Employment level
    Intermediate (1-3 years)
  • Employer industry
  • Job Reference
  • Closing Date
  • Date Published
  • Status

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