We are now recruiting a QA BMR Review Technician (12 months) to join our diverse QA team in Clonshaugh, Dublin.

Are you intrigued? Do you want to learn more?

A snapshot of your key responsibilities as a QA BMR Review Technician would be:

• Reviews BMRs for completion and accuracy.
• Reviews CPPs of BMRs to ensure there were no deviations from the filed process.
• Raise and support the completion of CAPAs, Non-conformances and Change Controls.
• Review, collate and submit the necessary documentation to support QP release of finished product in accordance with Annex 16.
• Responsible for the management of the retain system for samples and documents.
• Provide assistance in departmental and regulatory audits.
• Has the ability to train a colleague in a particular GMP procedure or related activity.
• A third level qualification in a scientific discipline, preferably a B.Sc./M.Sc.
• Pharmaceutical experience with good working knowledge of cGMP.
• Strong knowledge of FDA/EMEA regulatory requirements.
• Excellent organizational, communication and interpersonal skills.
• Ability to set and maintain the highest standards
  
  

AbbVie is committed to operating with integrity, driving innovation, transforming lives, serving our community, and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status.