Exciting Pharmaceutical Projects: Join a Centre of Excellence
QC Bioassay Analyst - Pharmaceuticals
This is an 11-month contract opportunity with the possibility of extension. Our pharmaceutical client has the largest centre in the industry worldwide, employing over 1000 people.
As a QC Bioassay Analyst, you will be involved in critical investment projects both on-site and remotely.
Responsibilities:
* Work under the direction of the Bioassay Manager / Associate Director, adhering to Company safety policies, cGMP, and cGLP.
* Maintain compliance with Global policies, procedures, and guidelines, as well as regulatory requirements while executing Good Manufacturing Practices (cGMP).
* Develop, implement, and maintain procedures that adhere to regulatory requirements.
* Ensure adherence to Quality Systems within the department on a daily basis.
Requirements:
* Knowledge of Irish, European, and International Codes, Standards, and Practices.
* Understanding of cGMP and Laboratory Quality Systems.
This role requires a strong understanding of regulatory/code requirements and laboratory quality systems. If you are interested in working with a Centre of Excellence in the pharmaceutical industry, please consider this opportunity.