Quality Specialist - Pharmaceuticals
This is a fantastic opportunity to work on a state-of-the-art fill-finish facility and the company's first stand-alone vaccine and biologics plant outside the US.
The role requires supporting Engineering activities through documentation generation, equipment and process investigations associated with GMP activities and completion of quality notifications.
You will be responsible for:
* SUPPORTING ENGINEERING ACTIVITIES THROUGH DOCUMENTATION GENERATION AND EQUIPMENT INVESTIGATIONS
* RAISING CAPAS AND CONDUCTING INVESTIGATIONS
* COMPLYING WITH MERCK GLOBAL POLICIES AND REGULATORY REQUIREMENTS
* SUPPORTING AND LEADING INTERNAL QUALITY AUDITS OF ENGINEERING DEPARTMENT
The ideal candidate will have a strong career history in pharma, familiarity with a highly regulated environment and experience working in a cross-functional environment. Knowledge of Six Sigma and Lean methodologies is also desirable.
The following qualifications are required:
* DEGREE QUALIFICATION OR EQUIVALENT MIN LEVEL 7 (SCIENCE, ENGINEERING, TECHNICAL)