Join a leading pharmaceutical client with the largest veterinary vaccine development and production centre worldwide.
This Centre of Excellence employs over 1000 people and is seeking a Quality Control (QC) Bioassay Analyst to join their team on an 11-month contract with possible extension.
Responsibilities:
* Work under the direction of the Bioassay Manager or Associate Director, adhering to company safety policies, cGMP, and cGLP guidelines.
* Ensure compliance with global policies, procedures, and regulatory requirements while executing Good Manufacturing Practices (cGMP) in daily activities.
* Develop, implement, and maintain procedures that meet appropriate regulatory requirements.
* Maintain adherence to quality systems within the department on a daily basis.
Requirements:
* Knowledge of regulatory codes, including Irish, European, and International standards and practices.
* Understanding of current Good Manufacturing Practices (cGMP).
* Experience with laboratory quality systems.
Company Overview:
Our client is a world-renowned pharmaceutical company committed to delivering high-quality products and services. With a strong focus on innovation and excellence, they offer a dynamic work environment that fosters growth and collaboration.