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QUALIFIED PERSON
Company:CPL CORK |
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Job Reference Number |
13502652 |
Client ID: |
RI/JO090550 |
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Posted On: |
Jun 22 2009 |
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Location: |
CORK |
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Job Type: |
Permanent |
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Salary: |
NEGOTIABLE |
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Duties & Responsibilities :
• Ensure batches are certified/dispositioned appropriately in accordance with all required regulations and in compliance with marketing authorisation.
• Provide Quality leadership, direction and governance for the specific area of responsibility.
• Manage quality-related matters specific to area of responsibility.
• Is responsible for approving appropriate quality-related documents. An approval signature confirms that company, GMP and appropriate regulatory requirements have been met.
• Performs ongoing monitoring that includes:
- monitoring of quality systems, the self-inspection program, verification of the effective implementation of key GMP programs and, review of systems that impact safety, identity, strength, purity, quality (SISPQ) to ensure that they operate in a state of control.
Reports to : Quality Assurance (QA) Team Leader
Candidate Requirements
• 2 years experience operating as a QP or in a licensed manufacturing facility.
• BSc, MSc or PhD in Science, Engineering or related discipline. Must hold Higher Diploma in Pharmaceutical Manufacturing Technology (QP).
To apply please send your CV in to Rory Walsh (Senior Recruitment Consultant, Science) at rory.walsh@cpl.ie or call me for a confidential discussion on 021 4626112.
