We are now recruiting a QA BMR Reviewer 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.
Qualifications :
- A third level qualification in a scientific discipline preferably a ./.
- 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.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
We are now recruiting a QA BMR Reviewer to join our diverse QA team in Clonshaugh Dublin.Are you intrigued Do you want to learn moreA 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 dev...
We are now recruiting a QA BMR Reviewer 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.
Qualifications :
- A third level qualification in a scientific discipline preferably a ./.
- 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.
Additional Information :
AbbVie is an equal opportunity employer and is committed to operating with integrity driving innovation transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more visit & Puerto Rico applicants seeking a reasonable accommodation click here to learn more:
Work :
No
Employment Type :
Full-time
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