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Republic of Ireland
Limerick
Dublin South
Cork
Galway
Cork
Cork
Limerick
Limerick
Galway
Galway
Dublin
Galway
Galway
Dublin South
Galway
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Limerick
Dublin
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Kildare
Limerick
Limerick
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Dublin
Republic of Ireland
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Republic of Ireland
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Cork
Galway
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Dublin South
Westmeath
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Dublin
Limerick
Galway
Limerick
Donegal
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Wexford
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Dublin South
Dublin
Limerick City
Wexford
Cork
Dublin
Donegal
Tipperary
Dublin
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Dublin
Dublin
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Galway
Limerick
Cork
Dublin
Galway
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Louth
Dublin South
Republic of Ireland
Dublin
Dublin South
Cork
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Dublin South
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Galway
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Longford
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Roscommon
Cork
Galway
Kerry
Dublin South
Dublin South
Galway City
Longford
Kildare
Republic of Ireland
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Limerick
Qualified Person - Pharmaceutical
| Reference: | AOORASYW-885602 | Location: |
Cork Cork City |
| Qualification: | Degree | Experience: | 5-7 Years |
| Job Type: | Permanent | Salary: | Not Disclosed |
QA Specialist/QP
Description
My client manufactures and distributes X-ray and MRI Contrast Media for internal and external customers worldwide. As part of the Pharmaceutical Diagnostics (PDx) business of the company, we support the PDx vision of being the best-in-class supply chain delivering the right dose to the right patient at the right time. At their campus at Cork, they employ approximately 600 staff and are a 24/7 operation exporting to 93 markets worldwide.
As QA Specialist/QP, you will manage and drive the site QA systems in close cooperation with other specialists in the QA Product Quality Team. You will coordinate and execute all QA duties relating to QP batch release and communicate all issues.
Responsibilities
• Coordination of the certification of finished product batches to the market as required under the EU directive 2001/83/EC
• Ensure that the batch and its manufacture comply with GDP, GMP, Regulatory Licences and Marketing Authorization
• Maintain oversight of deviations, CAPA & Change Controls and ensure any issues which have a regulatory impact are notified to health authorities and mitigated as required
• Continuous improvement of the manufacturing and quality systems – Identifying and building in efficiencies as necessary from a systematic and compliance perspective
• Coordinate support for operations in general troubleshooting and problem solving, providing technical direction and guidance to support overall business needs
• Maintain up-to-date knowledge of pharmaceutical legislation and industry best practice.
Qualifications and experience
• 3rd level qualification in Science / Engineering discipline or equivalent knowledge or experience
• Significant experience within a GMP / QA environment in a pharmaceutical company or similar regulated environment
• Eligible to act as a Qualified Person in line with local and EU directives.
Desired Skills
• Ability to create and maintain effective interpersonal relationships with all levels of personnel within all cross functional departments in the organization
• Excellent communication, negotiation and risk based decision making skills, promoting openness, dialogue and collaboration
• Results oriented with a strong ability to effectively troubleshoot and problem solve issues
• Promote a continuous improvement culture.
Eligibility requirements
- A good level of English and a valid work permit
- Level 8 degree that enables you to be QP eligible (MSc Pharm for example)
If you are interested in this role, contact Alan on [email protected] / 087 365 7522
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