QC Bioassay Analyst - Pharmaceuticals 11-Month Contract + Possible Extension
We are seeking a skilled QC Bioassay Analyst to join our team in the development and production of veterinary vaccines.
Responsibilities:
* Work as directed by 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) in day-to-day activities.
* Develop, implement, and maintain procedures that comply with appropriate regulatory requirements.
* Guarantee adherence to all 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.