Enter a job title or keyword

Quality Compliance Specialist 12 Month FTC

Grifols


Job Location:

Dublin - Ireland

Monthly Salary: Not provided by the employer
Posted: 22 August 2026 (27 days ago)
Application Deadline: 19 November 2026
Vacancies: 1 Vacancy

Job Summary

Would you like to join an international team working to improve the future of healthcare Do you want to enhance the lives of millions of people Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop produce and market innovative medicines solutions and services in more than 110 countries and regions.

At Grifols we believe that diversity adds value to our business our teams and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

Position Summary

The Quality Compliance Specialist is responsible for the execution of a variety of compliance requirements within the Quality Management System (QMS) of the site. This role is key in maintaining and updating compliance activities throughout the site. While ensuring managements awareness of the systems performance. The execution of all applicable requirements related to QMS Corporate requirements Regulatory compliance and applicable Grifols Policies or Procedures.

What Youll Do

  • Potential Responsibilities at management discretion:
    Provide Reports to site in relation to Quality Management System (QMS) as required.
    Provide regular reports on sites metrics to appropriate management
  • Management and ownership of:
    Quality system integration
    Data Integrity system
    Applicable training requirements (i.e. GMP introductory and refresher training)
    Quality Risk Management
    Supplier management system
    Support the completion and execution of Site Quality Council and Annual Product Reports
    Communicate with cross functional departments sites compliance and quality systems issues
    Supporting or Conducting audits of suppliers/outsourced providers where applicable
    Supporting the coordination of self-inspection system in GWWO where applicable
    Provide support ensuring external audit readiness and during external audits and corporate internal audits
    Ensures the corrections of findings risks and recommendations are promptly and thoroughly incorporated into the quality systems
    Identifies and shares Best Practices
    Participate in investigations of quality system issues and drives CAPA implementation to ensure CAPA findings risks recommendations and outcomes are appropriate and are clearly documented and communicated
    Trends analyses and reports on quality data to improve product and process Quality; develop recommendations based on data analyses
    Responsibilities include managing and coordinating (not Exhaustive)
    Supplier qualification process supplier complaints and supplier agreements
    Quality Risk management
    Data Integrity management
    Other activities related to QMS.
  • Other additional duties may be assigned by the Quality Systems & Compliance Management if required.

What Youll Bring

  • Competence in Microsoft packages specifically word excel and PowerPoint
  • Ability to work proactively on own initiative
  • Excellent technical writing and analytical skills
  • Flexibility
  • Results orientated
  • Process improvement and procedure writing expertise
  • Experience of conducting audits
  • Detail oriented well organized and able to work independently and in teams
  • Good communication skills both verbal and written
  • Flexible able to adapt quickly to change in a fast-paced environment
  • Solid problem-solving skills
  • Previous experience in auditing
  • Previous experience in health authorities audits
  • Qualifications:
  • Bachelors degree (B.A./B.S.) or equivalent
  • Two to four years experience in the pharmaceutical and/or biotechnology-based industry (as deemed necessary by hiring manager).
  • Experience with assisting or managing QA audits and inspections.
  • Good working knowledge of pertinent regulations and site SOPs.
  • Demonstrates strong communication and facilitation skills.
  • Certification in auditing will be considered an advantage.
  • MSc in a science pharmacy or related discipline an advantage

Our Benefits Include

  • Highly competitive salary
  • Annual performance-based bonus
  • Share options scheme
  • Group pension scheme with company matching contributions
  • Private Medical Insurance
  • Ongoing opportunities for career development
  • Succession planning and internal promotion opportunities
  • Education assistance
  • Wellness and social activities
  • Collaborative and inclusive working environment

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to applywere excited to hear from you.

Location: Grange Castle International Business Park Clondalkin Dublin Ireland.

Location: Grange Castle International Business Park Clondalkin Dublin Ireland

Learn more about Grifols


Required Experience:

IC


About Company

Company Logo

Explore Grifols' comprehensive, innovative and patient-centric biopharma and healthcare solutions.

View Profile View Profile