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Athlone
Carlow
Galway City
Galway
Republic of Ireland
Limerick
Carlow
Galway
Galway
Tipperary
Republic of Ireland
Tipperary
Carlow
Dublin
Carlow
Cork
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Dublin
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Dublin
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Galway
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Dublin
Dublin
Limerick
Dublin
Limerick
Tipperary
Clare
Limerick
Cork
Galway
Galway
Tipperary
Dublin
Galway
Limerick
Westmeath
Tipperary
Cork
Dublin
Limerick
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Dublin
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Dublin
Dublin
Galway
Dublin
Dublin
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Republic of Ireland
Wexford
Louth
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Dublin
Republic of Ireland
Limerick
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Tipperary
Carlow
Dublin
Dublin
Carlow
Limerick
Dublin
Carlow
Republic of Ireland
Limerick
Galway
Galway
Clare
Carlow
Dublin
Limerick
Dublin
Dublin
Dublin
Galway
Carlow
Dublin
Dublin
Clare
Westmeath
Carlow
Galway
Carlow
Dublin
Galway
Carlow
Cork
Carlow
Dublin
Dublin
Galway
Galway
Dublin
Dublin
Dublin South
Republic of Ireland
Dublin
Galway
Carlow
Republic of Ireland
Dublin
Carlow
Carlow
Dublin
Tipperary
Tipperary
Dublin
Dublin
Louth
Dublin
Galway
Louth
Galway
Athlone
Dublin
Dublin
Limerick
Galway
Galway
Dublin
Galway
Galway
Dublin
Galway
Carlow
Galway
Galway
Louth
Carlow
Wexford
Dublin South
Limerick
Galway
Limerick
Tipperary
Dublin
Tipperary
QC Separation Analyst
Reference: | SMC34796 | Location: |
Cork |
Qualification: | Degree | Experience: | See description |
Job Type: | Fixed Term Contract | Salary: | Not Disclosed |
We’re currently recruiting for an exciting opportunity with an award-winning Pharmaceutical organization based in Cork. This is an excellent position for anyone who is looking to join a leading multinational who are one of the best at what they do.
Duties
• Achieves a high level of competency in laboratory methods and procedures to support in process and release testing of biotechnology products.
• Review and approval of laboratory test results.
• Performs analytical testing activities in relation to method validation and technical transfer activities to ensure that all methods meet ICH, USP and EP guidelines.
• Executes validation, operation, maintenance, calibration and troubleshooting of equipment and it’s associated software.
• Write/executes reports and reviews IQ/OQ and PQ protocols to ensure that all relevant equipment is qualified for cGMP use.
• Ensures that all testing is completed, reviewed and approved within agreed turnaround times.
• Ensures QC activities are carried out in compliance with product license commitments, cGMP and company quality standards.
• Trains other QC analysts in laboratory methods and procedures when required.
• Writes/updates and reviews TMs, SOPs and WIs as required.
• Writes and reviews invalid assays, non-conformances and deviations as required.
• Actively participates in JSI lean initiatives such as Kaizen, 6S and Gemba.
• Is an active member of the QC group and provide assistance with other group activities as required.
• Communicates relevant issues to the QC Team Leader promptly.
• Maintains and develops knowledge of analytical technology as well as cGMP standards.
Education & Experience
• BSc (Honors) in a scientific/technical discipline.
• 2 years’ experience in a QC laboratory-testing environment within the biological and/or pharmaceutical industry.
• HPLC, Capillary Electrophoresis, UPLC/ Mass Spec experience
If interested in this posting please feel free to contact Sean McCarthy on +353 (0)87 798 8480 or [email protected] for further information.
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