Description
A global pharmaceutical manufacturing company is looking for a QA Investigations Manager to support the implementation of an improved deviation management strategy on one its sterile production sites.Location: near Oslo, Norway
Duration: 6 months
Role and Responsibilities:
• Improve the deviation investigation strategy together with different stakeholders on the site
• Facilitating and assisting root cause analyses and the closure of deviations
• Overseeing the implementation and management of CAPAs on existing deviations
• Providing general support to an upcoming FDA audit
Requirements:
• Quality Assurance background within pharmaceutical manufacturing
• Experience conducting deviation investigations, root cause analysis and CAPA implementation
• Experience with sterile filling processes
• Knowledge of FDA cGMP standards
• Able to foster relationships with different stakeholders on site
This is a challenging role which will make a long term impact on the effectiveness of a manufacturing plant. Apply now to be considered.