QC Bioassay Analyst - Pharmaceuticals - 11-Month Contract + Possible Extension
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 Bioassay Analyst.
This is a fantastic opportunity to be involved with critical investment projects both on-site and remotely.
Responsibilities:
1. Work as directed by the Bioassay Manager / Associate Director, according to Company safety policies, cGMP and cGLP.
2. Drive compliance with Global policies, procedures and guidelines, and regulatory requirements while executing Good Manufacturing Practices (cGMP) in day-to-day activities.
3. Comply with Global Policies, Procedures and Guidelines, regulatory requirements, and execute current Good Manufacturing Practices (cGMP) in day-to-day activities.
4. Develop, implement, and maintain procedures that comply with appropriate regulatory requirements.
5. Ensure that all Quality Systems within the department are adhered to on a daily basis.
What they need:
1. Knowledge of regulatory/code requirements to Irish, European, and International Codes, Standards, and Practices.
2. Knowledge of cGMP.
3. Laboratory Quality Systems.
If this role is of interest to you, please apply now!
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