QA Specialist, Medical Devices & Compliance

QCS Staffing

Dublin

On-site

EUR 45,000 - 60,000

Full time

14 days+
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Job summary

QCS Staffing is seeking a QA Specialist to support a life-changing pharmaceutical organisation in Dublin on an initial 12‑month contract. The role focuses on ensuring compliance and readiness for regulatory inspections within the Medical Device/Combination Product space.

You will help progress documentation, support audit activities, and analyze QMS data to support Management Review meetings and actions. A regulated industry background and experience with electronic QMS tools are essential.

Qualifications

  • Bachelor's degree or equivalent in a regulated industry.
  • Knowledge of regulatory/compliance requirements for medical devices (FDA QMSR 21 CFR Part 820, Part 4; ISO 13485; EU 2017/745; ISO 14971).
  • Experience using electronic QMS / document management systems (e.g., Veeva Vault).
  • Experience managing quality/compliance projects in a regulated medical device environment.

Responsibilities

  • Support the Medical Device Quality Team in progressing updates and release of documents & records in the document management system.
  • Support Combination Product Audit readiness initiatives and during audits.
  • Support Notified Body and Health Authority inspections and compliance.
  • Collect/collate QMS data and perform data analysis for periodic Management Review reports, meetings, minutes and actions.

Skills

Quality project management
Regulatory knowledge

Education

Bachelor's degree or equivalent

Tools

Veeva Vault

Job description

QCS Staffing is seeking a QA Specialist to support a life-changing pharmaceutical organisation in Dublin on an initial 12‑month contract. The role focuses on ensuring compliance and readiness for regulatory inspections within the Medical Device/Combination Product space.

You will help progress documentation, support audit activities, and analyze QMS data to support Management Review meetings and actions. A regulated industry background and experience with electronic QMS tools are essential.

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