QP

Cork  ‐ Onsite
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Description

Permanent QP / Qualified Person needed for global pharmaceutical company based in Cork.
As the QP you will be responsible for the release of finished products and management of manufacturing processes and quality systems. Mentoring and advising team of QA specialists.
Duties include:
* Review of batch manufacturing and quality control data to release product.
* Manage product and process investigations.
* Represent QA in a wide range of activities including site projects and routine validation activities to ensure continued compliance with manufacturing and product licenses and GMP requirements.
* Provide QA oversight for analytical work and laboratories to ensure continued compliance with regulatory guidelines, GMP and GLP.
* Maintenance of Quality Systems
* Participate and support the Internal audits and external regulatory inspections
* Participate in vendor audit programme where required
* Contribute to the development of policy within the QA organization
* Maintain up-to-date knowledge of pharmaceutical legislation and industry best practicePharmacy / Science degree5 years experiences QA within the Pharmaceutical IndustryThis is a permanent opportunity
Requirements:
5 years in QA in the pharmaceutical industry
QP experience or QP eligibility
Salary is depending on experience up to EUR65,000 + benefits.
If you are interested in a new role within QA contact me Anna Mooney on or apply with your cv.
I am also looking for permanent QPs in Dublin and Athlone.
Start date
04/2016
From
Real Staffing
Published at
26.02.2016
Project ID:
1078579
Contract type
Permanent
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