QA Manager
Role Purpose:
- We’re currently recruiting for an exciting opportunity with a rapid growing pharmaceutical organization based in Tipperary.
Core Duties and Responsibilities:
- Maintenance of External Supply Quality licenses as it relates to global GMP/GDP activities (MIA, ASR, WDA)
- Ensuring the review, and where appropriate, preparation and regular update of Quality Agreements
- Owner and approver of GMP/GDP QMS documents
- Support the annual Quality Management Review meeting and co-ordination of any actions from this meeting for implementation.
- QA approval of deviations/non-conformances ensuring deviations are fully investigated and that remedial measures are implemented to address the root cause of failures and relevant actions are taken to prevent their re-occurrence.
- QA approval of change control proposals (third party contractors and internal) and action plans.
- Coordinate mock recall task force team to test the recall process in accordance with governing procedures and issuance of report with recommendations and corrective action plans for any deficiencies identified.
Education & Qualifications Required:
- Bachelor’s Degree in a Science or similar Field
- 8+ years of quality and manufacturing experience in biotech or pharmaceutical industry
- Understanding of the applicable manufacturing/testing processes
- Ability to oversee multiple projects simultaneously
Please note, we do not require agency assistance with this role.
Apply Now
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Role Details:
| Job Title: | QA Manager |
| Location: | Tipperary |
| Type: | Contract |
| Date: | March, 2026 |
Role Details:
| Job Title: | QA Manager |
| Location: | Tipperary |
| Type: | Contract |
| Date: | March, 2026 |
Role Purpose:
- We’re currently recruiting for an exciting opportunity with a rapid growing pharmaceutical organization based in Tipperary.
Core Duties and Responsibilities:
- Maintenance of External Supply Quality licenses as it relates to global GMP/GDP activities (MIA, ASR, WDA)
- Ensuring the review, and where appropriate, preparation and regular update of Quality Agreements
- Owner and approver of GMP/GDP QMS documents
- Support the annual Quality Management Review meeting and co-ordination of any actions from this meeting for implementation.
- QA approval of deviations/non-conformances ensuring deviations are fully investigated and that remedial measures are implemented to address the root cause of failures and relevant actions are taken to prevent their re-occurrence.
- QA approval of change control proposals (third party contractors and internal) and action plans.
- Coordinate mock recall task force team to test the recall process in accordance with governing procedures and issuance of report with recommendations and corrective action plans for any deficiencies identified.
Education & Qualifications Required:
- Bachelor’s Degree in a Science or similar Field
- 8+ years of quality and manufacturing experience in biotech or pharmaceutical industry
- Understanding of the applicable manufacturing/testing processes
- Ability to oversee multiple projects simultaneously
Please note, we do not require agency assistance with this role.
Apply Now
"*" indicates required fields
