Job Title: QC Bioassay Analyst - Pharmaceuticals
Contract Duration: 11-Month Contract + Possible Extension
Job Summary
Are you interested in working with exciting pharmaceutical projects? Our client, a leading Centre of Excellence in veterinary vaccine development and production, is seeking a QC Bioassay Analyst to join their team.
Responsibilities:
* Work under the direction of the Bioassay Manager/Associate Director, adhering to Company safety policies, cGMP, and cGLP.
* Ensure compliance with Global policies, procedures, and guidelines, as well as regulatory requirements, while executing Good Manufacturing Practices (cGMP) on a daily basis.
* Maintain and develop procedures that meet relevant regulatory requirements.
* Verify adherence to Quality Systems within the department on a daily basis.
Requirements:
* Knowledge of regulatory/code requirements for Irish, European, and International Codes, Standards, and Practices.
* Familiarity with cGMP.
* Understanding of Laboratory Quality Systems.
About Us
Our client is a Centre of Excellence in veterinary vaccine development and production, employing over 1000 people worldwide. They are committed to innovation and excellence in their field.
If this opportunity interests you, please submit your application.