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Contact Info
Jack Caffrey
Life Science

01 507 9279
[email protected]
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Validation Lead
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QC Analyst

Reference:JSC00030731 Location: Cork
Qualification:DegreeExperience:See description
Job Type:Fixed Term ContractSalary: Not Disclosed
May be suitable for: QC Analyst

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.

This position is responsible for carrying out tasks and projects related to
equipment, lab utilities and testing procedures as required by Good
Manufacturing Practice (GMP). Partners with other Departments to ensure
that all QC testing activities are completed in an efficient manner.

General Responsibilities
• Achieves competency in laboratory methods and procedures.
• Trains other QC analysts in laboratory methods and procedures
• when required.
• 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 its associated software.
• Writes, executes, reports and reviews IQ/OQ and PQ protocols to
• ensure that all relevant equipment is qualified for cGMP use.
• Performs routine and non-routine analytical testing activities.
• Review and approval (where appropriate) of laboratory test
• results.
• Ensures that testing and results approval are completed within
• agreed turnaround times.
• Writes and reviews laboratory TMs, SOPs and WIs as directed by
• company policy.
• Ensures QC activities are carried out in compliance with product
• license commitments, cGMP and company quality standards.
• Is an active member of the QC group and provide assistance with
• other group activities as required and communicates relevant
• issues to the QC Team Leader and Manager.
• Deals with non-conformances/ deviations in an accurate and
• timely manner.
• Deputizes for the QC Team Leader as appropriate.
• Maintains and develops knowledge of analytical technology as
• well as cGMP standards.
• In process control testing and activities to support the production
• units.

Qualifications and experience
• A third level qualification of a scientific/technical discipline is required.
HPLC or electrophoresis knowledge/experience
• Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
• Builds strong productive relationships.
• Demonstrates ability to work with teams and individuals
• Asserts personal ideas and opinions using persuasion toinfluence others
• Seeks opportunities to grow and develop professionally
• Uses best practices to improve business operations
• Holds self-accountable for compliant and flawless execution
• Takes personal responsibility for decisions that successfully build customer value
• Effectively manages and adapts to change
• Demonstrates the courage to stand alone on ideas and opinions that differ from others
• Listens effectively and remains open to other’s ideas.
• Works effectively with people that have diverse ss, talents and ideas
• Maintains the highest standards of ethical behaviour
• Treats people with dignity and respect