QC Analyst - Ireland, Carlow – 11 Month Contract
Do you want to be involved with exciting pharmaceutical projects?
When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a QC Analyst.
What you’ll do:
* Work as directed by the QC Manager / Associate Director, according to Company safety policies, cGMP and cGLP.
* Required to drive compliance with our Global policies, procedures and guidelines and regulatory requirements and execute Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
* Required to comply with our Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of day to day activities and all applicable job functions.
* Develop, implement and maintain procedures that comply with appropriate regulatory requirements.
What you’ll need:
* Knowledge of regulatory/ code requirements to Irish, European and International Codes, Standards and Practices.
* Knowledge of cGMP
* Laboratory Quality Systems
* Proficiency in Microsoft Office and job-related computer applications required
* Report, standards, policy writing skills required
* Bachelor’s Degree or higher preferred; ideally in a science related discipline.
If this role is of interest to you, please apply now!
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