Senior QARA Specialist

Werfen
Full-time Lliçà d'Amunt, Catalunya Business Operations Specialists
Posted:
March 01, 2026
Location:
Lliçà d'Amunt, Catalunya, Spain

Job Description

Overview

Within a medical device environment, work with the QARA Manager to ensure regulatory compliance and certification of software products.

Responsibilities

Key Accountabilities

  • Collaborate in maintaining the quality system documentation processes and procedures adopted by the company.
  • Investigate and resolve quality issues, implementing corrective and preventive actions to mitigate recurrence.
  • Coordinate and support the preparation of software technical documents appropriate for regulatory submissions.
  • Support the regulatory submissions for market authorization for medical device products.
  • Conduct internal assessments and audits to identify areas for improvement and ensure adherence to established procedures.
  • Facilitate the approval process for software releases.
  • Disseminating knowledge about the Quality System and regulatory requirements.
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    Job Overview

    Job Type: Full-time
    Location: Lliçà d'Amunt, Spain
    Posted: March 01, 2026
    Deadline: April 10, 2026